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Langue du site : Français - English
Réf : 28067
Evènement :Record Keeping Best Practices [FDA and EMA] Documentation

Date :Vendredi 09 Novembre 2018

Lieu :En ligne (Internet, Visioconférence, ...)

Type :Formation - Audience Internationale

Accréditation :--


 

Informations

Overview:
Good documentation Practices (GDP) is an essential factor that needs to be closely followed by the personnel in any regulated environment as a process for a successful project completion including observations of unanticipated responses that are required to be accurately recorded and verified.
 
Why should you Attend:
If you are involved in any product manufacturing, knowing GDP regulations is a must for you. It prevents a lot of errors and minimizes the chance of being spotted by the regulatory bodies in their audits.
 
Areas Covered in the Session:
Definition, Purpose, and Importance
General Rules and Principles of GDP
Requirements of Records
General Tips in GDP
Signature / initial and the meaning
Copying records
Document maintenance
 
Who Will Benefit:
Laboratory Personnel / Managers
Validation Specialists
Clinical Trial Personnel
Project Managers
 
Speaker Profile:
Dr. Afsaneh Motamed Khorasani PhD is a Medical and scientific Affairs expert and a Senior Scientist with a strong background in biomedical science and clinical trial/research. She has a tenured and diverse range of experience in medical affairs, basic and industrial clinical research and development, clinical trials, Medical and regulatory writing and intellectual property.
 
Event Fee: One Dial-in One Attendee Price: US $150.00
 
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com

Renseignements

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Annonceur

Compliance4All
Compliance4All is a professional trainings provider for the regulated industries. It offers professional trainings for regulatory compliance professionals and offers innovative strategic consulting and advice to a broad range of organizations. These services help them to be compliant with regulatory requirements. . Compliance4All [...]

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Précisions

Record Keeping Best Practices [FDA and EMA] Documentation Médecine - Pharmacie - Bio-Technologies
education, healthcare, training, medical conference
Tout public, Laboratory Personnel / Managers Validation Specialists Clinical Trial Personnel Project Managers
50 1 --
English

Divers

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