SBS - The best value in QMS software

Incretin Mimetic Drugs for Type 2 Diabetes: Possible Increased Risk

Thread starter Similar threads Forum Replies Date
S Drugs and Cosmetics Rules - India Other Medical Device Regulations World-Wide 0
M Can a PLD Registered in only one state sell prescription drugs to one in another state Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 0
M Informational Health Canada – Fees for Drugs and Medical Devices Medical Device and FDA Regulations and Standards News 0
M Informational USFDA Final Guidance – Coordinated Development of Antimicrobial Drugs and Antimicrobial Susceptibility Test Devices Medical Device and FDA Regulations and Standards News 0
P Sample of an end-use-letter for drugs according to FDA requirements US Food and Drug Administration (FDA) 2
O CFDA (China Food and Drugs Administration) Audit Finding Classifications China Medical Device Regulations 1
C How to Identify Counterfeit Medications (drugs)? US Food and Drug Administration (FDA) 5
S Why Drugs and generics are Approved while Biologics are Licensed ? US Food and Drug Administration (FDA) 1
J Vanessa's Law (Protecting Canadians from Unsafe Drugs Act) Canada Medical Device Regulations 1
Marc The Risks of Generic Drugs Coffee Break and Water Cooler Discussions 24
Ajit Basrur FDA Guidance Document - Expedited Programs for Serious Conditions ? Drugs & Biologics Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 0
H What is required to support changes to API Manufacturers in OTC Drugs? Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 2
Marc Urine Spills Staining Image of Wockhardt?s Generic Drugs Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 1
AnaMariaVR2 IMDRF Working With ICH on Harmonized Electronic Submission System for Drugs, Devices Other Medical Device Regulations World-Wide 0
G Manufacture of Drugs and Medical Devices in one location Manufacturing and Related Processes 7
V EO Sterilization of Drugs in Custom Convenience Kits Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 6
AnaMariaVR2 Public Health, Vaccines & Brain Drugs courses Training - Internal, External, Online and Distance Learning 0
D Differences between (c)GMP for Drugs and Medical Devices Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 3
C Testing for Chemotherapy Drugs Resistance ISO 13485:2016 - Medical Device Quality Management Systems 2
bio_subbu CDSCO issues Draft Guidelines for Approval of Clinical Trial & New Drugs Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 0
AnaMariaVR2 Drug Quality and Counterfeit Drugs in Nigeria & Handheld Spectrometers US Food and Drug Administration (FDA) 0
Q Health Canada - Licensed Devices now considered Drugs? Canada Medical Device Regulations 2
W How to manage drugs during a manufacturing process? ISO 13485:2016 - Medical Device Quality Management Systems 5
A Combination Product - Legacy Drugs and Reclassification 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 3
bio_subbu Medical Device Regulatory Guidelines ? TFDA (Tanzania Food and Drugs Authority) Other Medical Device Regulations World-Wide 1
Ajit Basrur Facts and Myths about Generic Drugs Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 2
Ajit Basrur CDSCO Guidelines for Port Officers on Imp and Export of Drugs & Cosmetics Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 0
D How to obtain NOC from DCGI (Drug Controller General of India) for importing drugs Manufacturing and Related Processes 6
C CMDCAS (Canadian Medical Devices Conformity Assessment System) for drugs ISO 13485:2016 - Medical Device Quality Management Systems 3
J India - Drugs Master File Notarisation for UK based Manufacturer ISO 13485:2016 - Medical Device Quality Management Systems 2
B Sport & Drugs - Where Do You Stand? Coffee Break and Water Cooler Discussions 30
O Cosmetics (otc) with Drugs - Expiration dates and three years stability / shelf life ISO 13485:2016 - Medical Device Quality Management Systems 1

Similar threads

Top Bottom