Mohamed Fazil M

3 Abonné

regulatory affairs master of pharmacy drugdevice combination product risk management risk journal club cdsco biologicals regulations & legislation the principles of ich gcp institutional review board independent ethics commitee investigator's brochure investigator sponsor ib iec irb ich e6 ich gcp e6 guidelines good clinical practice clinical research guidelines clinical research regulations saudi food & drug authority saudi arabia mra201t semester 2 matster of pharmacy auditing strategies audits unit 3 mra 102t document & regulatory writing 1st semester out of specifications (oos) quality management systems good regulatory practices

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Mohamed Fazil M

Présentations

OUT OF SPECIFICATIONS (OOS).pptx

AUDIT - AUDITING STRATEGIES.pptx

REGULATORY REQUIREMENTS FOR REGISTRATION OF DRUGS AND POST APPROVAL REQUIREMENTS IN SAUDI ARABIA.pptx

Good Clinical Practice Guidelines (ICH GCP E6).ppt

CDSCO Biologicals - Rules, Regulations, Guidelines and Standards for Regulatory Filing of Biologicals .pptx

Journal Club - Risk Management in Drug - Device Combination Product Development

J’aime

Good Clinical Practice Guidelines (ICH GCP E6).ppt

GPAT, Drug inspector, NIPER entrance

final year project

REGULATIONS FOR COMBINATION PRODUCTS AND MEDICAL DEVICES

Combination product

Regulation of biosimilar in India

Packaging designs and specifications

Sampling Techniques

Biostatistics

Medicinal and toilet preparations act and rules,1955 (excise duties)

Shikimik acid pathway

Antimicrobial preservative

Microbiological Contamination And Preservation Of Pharmaceutical Products

Management information system in health care

Pollution its types, causes and effects by naveed.m

Aquatic ecosystems