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Showing posts with label Certificate. Show all posts
Showing posts with label Certificate. Show all posts

Reproducible Research…free online course from John Hopkins


Learn the concepts and tools behind reporting modern data analyses in a reproducible manner. This is the fifth course in the Johns Hopkins Data Science Specialization.

About the Course

This course focuses on the concepts and tools behind reporting modern data analyses in a reproducible manner. Reproducible research is the idea that data analyses, and more generally, scientific claims, are published with their data and software code so that others may verify the findings and build upon them.  The need for reproducibility is increasing dramatically as data analyses become more complex, involving larger datasets and more sophisticated computations. Reproducibility allows for people to focus on the actual content of a data analysis, rather than on superficial details reported in a written summary. In addition, reproducibility makes an analysis more useful to others because the data and code that actually conducted the analysis are available. This course will focus on literate statistical analysis tools which allow one to publish data analyses in a single document that allows others to easily execute the same analysis to obtain the same results.

Course Syllabus

In this course you will learn to write a document using R markdown, integrate live R code into a literate statistical program, compile R markdown documents using knitr and related tools, and organize a data analysis so that it is reproducible and accessible to others.

Recommended Background

Course Format

There will be weekly video lectures,  quizzes, peer assessments.
As part of this class you will be required to set up a GitHub and an RPubs account. GitHub is a tool for collaborative code sharing and editing. RPubs is a web site for publishing data analyses from R. During this course and other courses in the Specialization you will be submitting links to files you publicly place in your GitHub account as part of peer evaluation. If you are concerned about preserving your anonymity you will need to set up an anonymous GitHub and RPubs accounts and be careful not to include any information you do not want made available to peer evaluators.

FAQ

How do the courses in the Data Science Specialization depend on each other?
We have created a handy course dependency chart to help you see how the nine courses in the specialization depend on each other.
Will I get a Statement of Accomplishment after completing this class?
Yes. Students who successfully complete the class will receive a Statement of Accomplishment signed by the instructor.
What resources will I need for this class?
A computer is needed on which the R software environment can be installed (recent Mac, Windows, or Linux computers are sufficient).

How does this course fit into the Data Science Specialization?

This is the fifth course in the Specialization. We strongly recommend that you first takeThe Data Scientist’s Toolbox and R Programming before taking this course.


Online Masters Degree in Clinical Research: Program Info


Healthcare professionals seeking advanced research degrees can enroll in online clinical research administration or management master’s programs. These degrees are delivered in a hybrid format; online curriculum completion is followed by a field-based internship. Read on to learn more about the curriculum and career options for this program.
Essential Information
Due to the hands-on requirement in the program, students can find master’s degree programs in clinical research in hybrid formats. Entrance into this field requires a bachelor’s degree, and some programs require applicants to be licensed. These programs include online coursework in clinical research and ethics, as well as an internship in the field that must be completed in person.

Online Master’s Degree in Clinical Program Overview
At the post-baccalaureate level, online clinical research degrees are commonly available in clinical research management or administration. These degree programs are designed for healthcare industry professionals interested in overseeing the complex processes of research trials. Students examine the scientific approach to developing medical products as well as the legal and ethical framework behind clinical trials.
Program enrollment is limited to students with bachelor’s degrees. Some programs may require students to be licensed clinical laboratory scientists. Related fields of study include biology and public health.

Program Information and Requirements

A typical clinical research program can be completed in two years. Coursework is delivered online through streaming audio and video applications, so a computer with access to the Internet is required. Though online programs are intended to be flexible, some may ask students to participate in scheduled forums or lectures. Many programs also require students to complete field-based internships under the guidance of a mentor.

List of Common Clinical Research Courses

There are no general education requirements for master’s degree students. All coursework deals specifically with issues related to clinical trial administration.

History of Clinical Research Course

Students explore the evolution of clinical research. Case studies are used to understand research goals, clinical processes and the various responsibilities of research team members.

Ethics and Legality in Research Course

Laws, ethical codes and government agencies regulate the clinical trial industry. Students examine the development of regulation in the field, with particular attention paid to rights of patients, conflicts of interest, scientific misconduct and independent review boards.

Research Data Analysis Course

Students learn how to interpret and organize different types of research data. Topics include qualitative analysis, trial proposals and written documentation.

Clinical Research in Practice Course

The process of researching and testing a pharmaceutical or medical product is discussed. Students explore how to create a project outline and conduct clinical tests.

Career Information for Graduates

Graduates of a master’s-level program in clinical research management or administration can obtain positions as research associates, coordinators or university teachers. Associates earned between $41,000 and $67,000 in 2009, while research coordinators made between $36,000 and $52,000, as reported byPayScale.com. University teachers took in between $36,000 and $59,000. The U.S. Bureau of Labor Statistics noted that job growth was expected to increase by 14% for clinical lab workers and by 15% for postsecondary teachers between 2008 and 2018 (www.bls.gov).

SOCRA Clinical Research Professional Certification

What About SOCRA Clinical Research Professional Certification Preparation and GCP Review Course?


SOCRA offers a 1 day in-person Clinical Research Professional Certification Preparation and GCP Review Course at various locations and dates in the U.S. and Canada. I had attended this course prior to my SOCRA CCRP exam in September 2013. Although the information presented on this course can be beneficial, and I would recommend this to anyone taking the exam, there are limitations to this course:
  • The cost for this preparation course is quiet considerable ($295 for SOCRA member, $370 for non-member). This is in addition to the cost of SOCRA membership ($75/yr) and the CCRP exam fee ($195).
  • The course is offered only a hand full of times per year in different locations. If you do not live near the location where the course will be held, traveling is involved. This means more costs for flight, hotel, car rental, and daily expenses.
  • The information is condensed into compact format in order to fit the 1 day time limit.
  • The information presented can be found from publicly available sources and is not a substitute to one’s own studying.
In my opinion, my own time in studying and taking notes from publicly available relevant information (various GCP trainings, CFR, ICH’s GCP, industry websites, etc.) and years of industry experience helped me much more. Another reason is that it was impossible for me to retain information from a 1 day compact course. It was useful for me to summarize key information from my own studying and absorb them at my own pace. If I were to attend this 1 day course without spending the time to study on my own prior to the exam, I would not have aced this exam or even passing it.

How ES’ SOCRA CCRP Study Guide Can Help Save You Time and Sanity

Instead of trying to plow through countless FDA regulations, guidelines, and industry practices, imagine if there is a Study Guide that helps summarize all those materials in an easy to digest format in bullet points.  Imagine if you can click and search different topics in seconds. Imagine if you can browse through and learn the information at your own place in the comfort of your home. Imagine if there are tips and suggestions from someone in the industry who had gone through the exam and aced it with flying colors.

Imagine no more

Imagine no more. I have compiled the note I took when I was studying for the SOCRA CCRP exam in September 2013. I have named it “ES’ SOCRA CCRP Study Guide” (ES stands for Ernie Sakchalathorn). From these notes, I was able to pass the SOCRA CCRP exam with a score of 96% (I answered 130 questions correctly out of 135 questions total, click HERE to see my score letter). Inside this Study Guide, there are:
  • 100+ Pages of Complete and Outlined Summaries of Materials for the SOCRA CCRP Exam
  • Sidebar Navigation Menu with Clickable & Expandable Links to Any Section
  • A Complete Bullet Outline of The Entire SOCRA CCRP Certification Process
  • Personal Tips From My Industry Experience Both As a CRC And a CRA
  • Updated to apply to new exam outline for exams to be held after June 1, 2014

Okay, so what’s the cost for this resource?

Well, how much is your time worth? How much are you willing to pay to not having to spend hours and hours searching through books and online resources or reading through documents such as Declaration of Helsinki, 21 CFR 312, or the ICH GCP from end to end? How much would you pay to get summarized information in easy to understand format plus inside tips from someone who took the exam who has years of industry experience? This Study Guide can save you precious time and may help you pass the exam and get the SOCRA CCRP certification you need.
If this resource existed back when I took the exam, I myself would pay $200 or more for it.  Your total investment cost for the ES’ SOCRA CCRP Study Guide is Retail price: $195. On Sale 25% Off $145!  Limited Time 50% Off Offer $95!
Compare that to the cost of the SOCRA’s in person Clinical Research Professional Certification Preparation and GCP Review Course, which can be either $295 for SOCRA member or $370 for non-member + the cost of getting there (flight + hotel + daily expenses). With the ES’ SOCRA CCRP Study Guide, you do not have to travel to get to the training course.  You simply study at the comfort of your home at your own pace!  Below are some more benefits of ES’ SOCRA CCRP Study Guide:
  • Instant Download! No More Waiting For Days For Your Guide!
  • No More Lugging Around A Thick Reference Book!
  • Electronic Format Saves Trees!
  • Easier to use. Easier to understand. Easier to Pass the exam!
By clicking “add to cart” you agree to the license agreement terms
To purchase multiple copies, please click HERE

Money Back Guarantee

You have 7 calendar days (more than enough time to browse through the entire Study Guide) to see if “ES’ SOCRA CCRP Study Guide” will help you pass the exam or not. If you ever feel that it has no absolute value and will not help you in your preparation, I will issue you a full, NO HASSLE refund for your investment. There is no risk whatsoever on your part. The burden to deliver is entirely on me.

To Get Started

It’s easy to get started. Just click the button below, select and enter payment information, and an email will be sent to your email address. In it will contain a link to download the book onto your computer. It’s that simple








Still Not Convinced? Want to see what it looks like inside? See the preview and read the first charpter (21 pages out of 106 total) below

Click here to read a sample chapter (21 out of 106 pages total)

I’m Ready to Start Studying

Click “ADD TO CART” Below to Get Your ES’ SOCRA CCRP Study Guide NOW!
By clicking “add to cart” you agree to the license agreement terms
To purchase multiple copies, please click HERE
Thanks for taking the time to read this. I wish you the best of luck on the exam.

GCP Certificates

The GCP Certificate of Completion has a new look! The completion certificate now lists the topics covered in the training as well as the completion and expiration dates for the certificate. Upon login and successful completion of all training modules, users will receive access to the new certificate.


TCPS2 CORE CERTIFICATE

The online tutorial TCPS 2: CORE (Course on Research Ethics) is an introduction to the 2nd edition of the Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans (TCPS 2). It consists of eight modules focusing on the guidance in TCPS 2 that is applicable to all research regardless of discipline or methodology.The purpose of TCPS 2: CORE is to provide an introduction to TCPS 2, primarily for researchers and, secondarily, for REB members.If this is your first time accessing TCPS 2: CORE, we suggest you click on the “CORE User Guide” for some tips on navigating the modules. There are also some other useful links below. Or you may go directly to the program by clicking the Log In button at right.
take exam for free

SOCRA Certification Exam


Certification Program Policies

Appeals

All appeals must be sent in writing to SOCRA Re: Certification Appeal by e-mail to office@socra.org , mailed to 530 West Butler Avenue, Suite 109 Chalfont, PA 18914 USA, or faxed to: (215) 822-8633.

Certification of Honesty

Falsification or misrepresentation of application information will invalidate the applicant’s certification status. This would include disapproval of the application or revoking of certification.

Confidentiality Statement

The SOCRA Certification Committee (the “Committee”) will take all reasonable measures to ensure that any material, reports, proceedings, and/or hearings related to the certification process shall remain confidential between the Committee and the candidate except as required by law, authorized in writing by the candidate, or as otherwise provided in the Committee’s Policies and Procedures.

Policy of Non-Discrimination

SOCRA does not discriminate on the basis of gender, race, color, age, marital status, sexual orientation, national origin, religion, or disability.

Special Needs / Disability Accommodation Policy

SOCRA – Society of Clinical Research Associates supports the intent of, and complies with the Americans with Disabilities Act (“ADA”). The Society of Clinical Research Associates will take steps reasonably necessary to make its assessment programs accessible to persons with disabilities covered by the ADA. An applicant may request a change in certification procedures or process due to a disability, handicap, or other reason. Appropriate and effective modifications and/or auxiliary aides will be provided to persons with such disability, handicap, or other reason unless doing so would impose an undue burden on the Society of Clinical Research Associates’ programs or fundamentally alter the measurement of skills or knowledge that the programs are intended to test. The Society of Clinical Research Associates certification examination does not discriminate against any candidate based on age, sex ethnic origin, religion, race, disability or marital status.
SOCRA will make every effort to accommodate applicants with special needs. If the applicant has special physical or testing needs due to a disability, handicap, or other reason, the applicant should attach a written request for accommodation with the certification application and at least six weeks in advance of the examination date. The written documentation should include a diagnosis or description of the disability or special need, the current level of functioning, and the requested accommodation. This statement must be written by a qualified medical professional (preferably a physician) and should be submitted on the letterhead of the medical professional or their institution or organization.
All special arrangements must be made and agreed upon in advance; such arrangements cannot be made at the time an examination is given. The Society of Clinical Research Associates will make the final determination as to the necessary accommodations for an individual with a verified disability.
For individuals with physical, visual or learning disabilities requiring an extended test time, there is no accommodation for untimed testing. Time and a half (6 hours) is appropriate accommodation for most disabilities. Double time (8 hours) may only be granted in special circumstances with the recommendation of qualified professionals.
At this time, SOCRA does not have an auditory examination for the visually impaired.

Test Center Policies & Procedures

Test Center Policies and Procedures may be found here.

Requirements for Maintaining Certification

Term of Certification / Certification Period
The certification period is 3 years, beginning on the date of most recent certification and ending on certification expiration date.   All CE must be accrued during this time period.
Maintenance of Membership
Membership must remain current during your certification period.   Annual renewal of membership and payment of membership renewal fees ($75/year) is required.  It is the responsibility of the certificant to maintain membership.  SOCRA, as a courtesy, sends membership renewal reminder by email 2 months prior to the membership expiration date.
Continuing Education Requirement
Certification of Clinical Research Professionals by SOCRA is based on a continuing process of professional experience and education. This program is dedicated to providing recognition and validation of the professional growth of the individual CCRP® to the healthcare community.
Certificants must have completed 45 hours (45 credits) of CE during their certification period. A minimum of 22 CE must be related to Clinical Research regulations, policy, etc. The remaining CE may relate to your Therapeutic or Professional Area. 1 CE will be awarded for the successful completion of the recertification quiz. Only educational hours may be claimed for CE; you may not claim CE credit for your work hours.
It is the responsibility of the certificant to maintain copies of program descriptions or agendas, and some form of verification of attendance such as a certificate of completion or letter of attendance or notice of grade, or class completion certificate. A random audit of programs submitted for CE credit will be conducted each year.
Recertification / Certification Renewal
In order to maintain active certification status, the CCRP® must apply for renewal of certification to the Certification Committee every three years.  More information regarding recertification can be found under the Recertification section of the website.

Continuing Education Requirements

Certificants must complete 45 hours (45 credits) of CE during their certification period.   A minimum of 22 CE must be related to Clinical Research regulations, policy, etc. The remaining CE may relate to your Therapeutic or Professional Area. 1 CE will be awarded for the successful completion of the recertification quiz.
It is the responsibility of the certificant to maintain copies of program descriptions or agendas, and some form of verification of attendance such as a certificate of completion or letter of attendance or notice of grade, or class completion certificate.  Please see CE Recordkeeping Requirements for more details.   A random audit of programs submitted for CE credit will be conducted each year.
Because of the diversity of SOCRA membership, a specific listing of approved CE programs will not be developed.  TheDescription of Acceptable CE overview serves as a guide for evaluating CE programs.
Certificants applying for recertification will be asked to sign an affidavit that verifies an accumulation of 45 hours of CE applicable to their work in clinical research.  Only educational hours may be claimed for CE; you may not claim CE credit for your work hours.
Accruing Continuing Education (CE)
All CE must be accrued during your certification period. We suggest that you keep an ongoing log of accrued CE to assure that you are keeping up to date on the requirements for maintenance of CE.   See CE Recordkeeping Requirements for more details on documentation requirements.
Categories of CE
The table below explains the breakdown of CE that you may claim within each CE category:
Category of CEDescription of CategoryAmount of CE AllowableTotal CE Required
Clinical Research Operations / RegulatoryCE related to clinical research regulations, policy, operations, etc.Minimum of 22 CEU may be claimed (no maximum)45 CE per 3 year certification period
Therapeutic / Professional AreaCE related to your specialty in research (therapy, treatment, etc.)No minimum
Recertification QuizCE for completing the self administered knowledge testOne (1) CE may be claimed
How to Calculate CE
  • As a rule, one (1) hour of activity = one (1) hour of CE. (45 minute presentation and 15 minute Q&A = 1 CE)
  • For example; One classroom hour of learning = One CE hour
  • For college courses; One (1) semester hour of college credit = ten (10) hours of CE
  • For Audio/Video; Tapes must be one hour in length for each hour claimed.
Descriptions of Acceptable CE
Please review the Description of Acceptable CE for more details and a guide for evaluating CE programs.

Descriptions of Acceptable CE

SOCRA’s requirements for recertification CE credit are quite general, as they pertain to research regulations, operations and management, and yet are also specific to the therapeutic area of the research in which the candidate participates. We therefore leave it to the candidate to determine whether a course or program is acceptable for the individual’s CE requirement, and we do not “validate” individual training courses/workshops/presentations.
Any question regarding the appropriateness of a program for CEUs may be e-mailed to SOCRA at: recertification@socra.org directed to the attention of the Certification Committee.
The Examples and Description of Acceptable CE table serves as a guide for evaluating CE programs.
Examples of acceptable programs include:
Types of ActivityDescription of ActivitySupporting Documentation Required (submit ONLY if audited)Maximum CEU Allowed
SOCRA Conference/ Workshop/ Chapter MeetingPrograms developed by SOCRA and SOCRA Chapter Meetings offering CECertificate of attendanceNo Maximum
Workshops at research facilities/sitesWorkshops at research facilities/sites or pharmaceutical company meetings encompassing subjects appropriate to clinical research.1. Agenda, AND2. Certificate of attendance and/or letter signed by supervisor
Web Based / Online CourseworkEducation related to clinical research or therapy
Other Seminars/ ConferencesSeminars, conferences, programs (applying to clinical research) that contribute to education or professional advancement
University/ College CourseworkCollege, university, or accredited independent study courses relevant to work in clinical research.1. Transcript showing completion of course, AND2. Syllabus/course description
Grand rounds, Tumor Boards, and IRB / IEC meetingsGrand rounds, tumor boards, and Institutional Review Board (IRB) / Independent Ethics Committee (IEC) meetings1. Agenda, AND2. Letter signed by supervisor stipulating learning hoursMaximum = 2 CE from all of these areas combined, per yearMaximum = 6 CE per certification period
Investigator / Site Initiation MeetingsCE can be claimed for the GCP training given at investigator meetings and site initiation visits (not for protocol specific training)1. Agenda, AND2. Letter signed by supervisor stipulating learning hoursNOTE: Only the GCP training sections of the meetings may be claimed.Maximum = 2 CE from all of these areas combined, per yearMaximum = 6 CE per certification period
Audio/VideoAudio and video recordings of CE programs related to clinical research (state, chapter or association meetings, area or local chapter meetings, etc.). Recordings must be one hour in length for each hour claimed.Summary of studied material (minimum 250 words)Maximum = 5 CE per yearMaximum = 15 CE per certification period
Self-Study / Journal ArticlesReading of journal articles and self study programs may be claimed in one-hour increments for each hour spent on the activity. 1 hour of this activity = 1 CESummary of studied material (minimum 250 words)Self-Study Articles with completed self-test exams do not require summaries.Maximum = 5 CE per yearMaximum = 15 CE per certification period
SOCRA Source Self Study article(s) offers 1 CE each. You may use articles from issues published during your certification period only.12 issues are published during a 3 year certification period.A copy of the completed SOCRA self-test exam for each article.
Active SOCRA officer, committee chair/memberActive participation in SOCRA as an elected officer, committee chair or active committee member for SOCRA or a SOCRA chapter.No documentation requiredNote: One year of such participation = one CE hourMaximum = 1 CE per yearMaximum = 3 CE per certification period

CE Recordkeeping Requirements
Recordkeeping
CE Documentation Requirements
It is the responsibility of the applicant to maintain copies of certificates of completion/attendance, OR program descriptions/agendas from the CE activity and a form of verification of attendance. If a formal certificate of completion or attendance is not available, please send one form of verification with the meeting description or agenda.
Certification may include any one of the following forms:
letter from meeting host which should verify attendance and hours of CE,
copy of official meeting sign-in sheet,
personal name tag with logo or name of program host,
notice of grade received or class transcript
Examples of items that DO NOT qualify as proof of meeting attendance include: notification of meeting, flight schedules, boarding passes, hotel receipts. Such items cannot assure an auditor that a candidate attended a program.
CE Tracking Tool
SOCRA created an excel based tool that members may download to help log and track their continuing education (CE) hours. We strongly suggest that certificants use this log to track their CE. The completed spreadsheet can then be submitted with the recertification application and quiz when applying for recertification. Click here to download the CE Tracking Log.

CE Documentation Retention Requirements
A CE tracking log may be downloaded from the SOCRA website to assist you in keeping track of your CE. Please retain all original certificates of attendance and documentation for 2 years after your certification period ends. The certificates of attendance and documentation will not be submitted with your recertification application. However, if selected for recertification audit, these certificates of attendance and documentation will need to be submitted. If you are unable to produce this supporting documentation at that time, your certification will be revoked. We suggest that you also retain a copy of your recertification application and CE tracking log submitted with your recertification application. A recertification audit is performed in the spring of each year, selecting up to 10% of the previous year’s recertification applications.

Request for SOCRA CE for Courses / Workshops
SOCRA’s requirements for recertification Continuing Education credit are quite general, as they pertain to clinical research regulations, operations and management, and to the therapeutic area of the clinical research in which the candidate participates. We therefore leave it to the candidate to determine whether a course or program would be acceptable for SOCRA’s CE requirement. SOCRA does not “validate” individual training courses/workshops.

Organizations offering courses may use the following text in their brochure/announcement:
“The Society of Clinical Research Associates (SOCRA – www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for recertification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program offers __ hours of CE credit.”

Renewal of Certification

Certification of Clinical Research Professionals by SoCRA is based on a continuing process of professional experience and education. The CCRP Recertification Program is dedicated to providing recognition and validation of the professional growth of the individual “CCRP®” to the healthcare community. The goal is to assure the safety of human research participants and improve the health of people around the world.
An overview of information regarding CCRP maintenance, continuing education requirements, and recertification can be downloaded here.
Certification Maintenance
During the 3-year certification period, certificants must follow the requirements for maintenance of certification.  TheMaintenance of Certification section of the website outlines the:
Recertification / Certification Renewal
In order to maintain active certification status, the CCRP® must apply for renewal of certification to the Certification Committee every three years.
The requirements for recertification include:
  • Current Certification and Current Membership  – A certificant wishing to recertify must be a member in good standing with a current certification. When a membership lapses, the CCRP® credential will automatically be suspended/removed.
  • Application for Recertification – A certificant wishing to recertify must complete the application for recertification, CE log and quiz.   These documents, along with the recertification processing fee (currently $100 USD), must be submitted to the SOCRA office prior to the certification expiration date.  More details may be found on under the Applying for Recertification section of the website.

Applying for Recertification

In order to maintain active certification status, the CCRP® must apply for renewal of certification to the Certification Committee every three years.
Recertification Reminder Packet
A recertification reminder packet is mailed to the certificant 2 ½ months before their certification expiration date.   The packet includes a recertification application, recertification quiz, and answer sheet.   If you do not receive the recertification packet by mail at least 2 months before your certification expiration date, please contact the SOCRA office.
Recertification Application Submission
To apply for recertification, applicant’s must complete and submit the following to the SOCRA administrative office BEFORE their certification expiration date:
  • Recertification Application – included in the Recertification Reminder Packet or may be downloaded here
  • Recertification CE log – A log of completed continuing education must be submitted with your recertification application packet.   This log must include the required forty-five (45) contact hours of continuing education, applicable to work in clinical research, during the period after the most recent certification date.  Please review the Continuing Education Requirements for more detailed information.  You may also download the CE Tracking Log, an excel based tool for logging and tracking continuing education (CE) hours.
  • Recertification Knowledge Quiz – The quiz will be sent to you with your recertification packet.  The quiz is open-book but must be completed independently.  Please be sure to select only one answer per question. It is suggested that you include the source to the answer on the test answer sheet.
  • Recertification Processing Fee – Submission of the $100.00 recertification processing fee in U.S. Funds to the SOCRA office.
* A printable version of the Recertification Application and Requirements for Maintaining your Certification may also be downloaded here.

Recertification Audit

An audit is performed in the spring each year selecting up to 10% of the previous year’s recertification applications. If selected for recertification audit, your recertification application, CE tracking log, and supporting documentation (including certificates of attendance and other documentation) will need to be submitted. If you are unable to produce this supporting documentation at that time, your certification will be revoked. For example, if you re-certify in February of 2013, you may be selected for audit in the spring of 2014.

About Blogger:

Hi,I,m Basim from Canada I,m physician and I,m interested in clinical research feild and web development.you are more welcome in our professional website.all contact forwarded to basimibrahim772@yahoo.com.


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