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Site language : English - Français
Ref : 27654
Event :Highlights of FDA GLP Regulations and the (Roles) and Responsibilities

Date :Monday September 10th, 2018

Location :Online (Internet, Videoconferencing, ...)

Type :Education - International audience

Accreditation :--


 

Further information

Overview: 

This 3 hour GLP virtual seminar will discuss various GLP regulations (FDA/OECD GLP's) along with highlighting roles and responsibilities of management and key personnel involved in drug development, safety & toxicity evaluation and QAU function in GLP testing facilities.

Why should you Attend: This 3 hour GLP Webinar will cover some of the major requirements, definitions and elements of the various GLP regulations, and the FDA/OECD GLP's. it will discuss the strategies to apply in effective implementation of a compliant GLP program with involvement and interactions and Case Studies and group exercise included in this highly interactive course presentation.

Areas Covered in the Session:

  • Introduction: Background of GLP's
  • Quality System Perspectives
  • Organization and Personnel
  • QAU: Audits and Responsibilities
  • Facilities
  • Study Conduct

Who Will Benefit:

  • Study Directors
  • Managers
  • Supervisors
  • Validation Managers
  • GLP Coordinators
  • QAU Personnel

Speaker Profile

Dr. Shib Mookherjea is a globally acclaimed speaker and consultant and has extensive experience in R&D, quality assurance, and quality management and teaches Methods Development, Validation Procedures, and Conformity Assessment in the Analytical Laboratory; Qualification and Validation of Laboratory Instruments and Equipment for Regulatory and QS Compliance (IQ, OQ, PQ); and the webcast Cleaning Validation and Compliance Issues for Pharma, Biotech and Medical Device Industries.
https://www.compliance4all.com/control/w_product/~product_id=502114LIVE?channel=doctorama_Sep_2018_SEO

Speaker Profile 


Dr. Shib Mookherjea is a globally acclaimed speaker and consultant and has extensive experience in R&D, quality assurance, and quality management and teaches Methods Development, Validation Procedures, and Conformity Assessment in the Analytical Laboratory; Qualification and Validation of Laboratory Instruments and Equipment for Regulatory and QS Compliance (IQ, OQ, PQ); and the webcast Cleaning Validation and Compliance Issues for Pharma, Biotech and Medical Device Industries.

Further information

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Announcer

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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Details

Highlights of FDA GLP Regulations and the (Roles) and Responsibilities Pharmacy - Medicine - Bio-Technologies - Infectious Diseases - Hygiene - National Health - Public Health
education, online training, fda, fda regulations, fda compliance training
Professionals, Supervisors Validation Managers GLP Coordinators
50 1 --
English

Other

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