GMP (Good Manufacturing Practices) essential information URL

Thread starter Similar threads Forum Replies Date
M Good Manufacturing Practices (GMP) for the Aerospace Industry AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
A GMP (good manufacturing practices) presentation materials 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
G Penalties for inadequate FDA GMP (Good Manufacturing Practices) System US Food and Drug Administration (FDA) 6
L GMP (Good Manufacturing Practices) for Wind Turbine Manufacturing and Exporting Other ISO and International Standards and European Regulations 3
G Armenia adopts GMP (Good Manufacturing Practices) - Armenian Health Authorities Other Medical Device Regulations World-Wide 0
S Please share a SOP on Medical Device Good Manufacturing Practices (GMP) US Food and Drug Administration (FDA) 8
N CFR 210 & CFR 211 - Major Differences to EU GMP (Good Manufacturing Practices) Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 2
D GMP (Good Manufacturing Practices) for IVD Manufacturer ISO 13485:2016 - Medical Device Quality Management Systems 12
M Training Basic GMP (Good Manufacturing Practices) to New Employees ISO 13485:2016 - Medical Device Quality Management Systems 5
A Good Manufacturing Practices (GMP) for Spices Food Safety - ISO 22000, HACCP (21 CFR 120) 4
R Good Manufacturing Practices - How you document your GMP's - GHP's and how detailed US Food and Drug Administration (FDA) 8
jkuil Calibration before and after relocation of GMP manufacturing equipment Calibration Frequency (Interval) 7
R Wooden Pallets in GMP Manufacturing Space Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 5
S GMP guideline for Manufacturing of Inhaled Dosage Forms Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 2
B GMP Compliant Flooring for Food Manufacturing unit Food Safety - ISO 22000, HACCP (21 CFR 120) 8
W Requirements of Contract Manufacturing in respect to GMP? ISO 13485:2016 - Medical Device Quality Management Systems 13
C GMP question - New pharma/drug manufacturing facility certification timeline/sequence Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 8
S HACCP and GMP+ B2 training questionarie Food Safety - ISO 22000, HACCP (21 CFR 120) 0
V Anyone have templates for FDA GMP Guidelines for supplement manufacturers? US Food and Drug Administration (FDA) 0
J Non_GMP (PIC/S 010) production in a GMP area ? Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 0
H OTC DRUG Private Labelling Distributor: GMP REQUIREMENT ISO 13485:2016 - Medical Device Quality Management Systems 0
P Product Quality Review API-GMP Manufacturing and Related Processes 0
N ISO 22716 - GMP Training for GMP trainer Other ISO and International Standards and European Regulations 2
pbojsen ISO 13485 Requirements versus FDA product classification and GMP exemptions - Audits ISO 13485:2016 - Medical Device Quality Management Systems 5
M Europe GMP medical devices - Combination products - Ancillary medicinal substance CE Marking (Conformité Européene) / CB Scheme 4
E Qualification for non gmp service providers Supplier Quality Assurance and other Supplier Issues 1
A Interpretation of GMP Requirements for class 1 medical device manufacturer (device GMP exempt, only General controls applicable) 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 4
O ISO 13485 vs. GMP - Comparison matrix wanted EU Medical Device Regulations 4
E Preparing for the ASQ CPGP (GMP professional exam), how to revise and remember the vast syllabus? ASQ - American Society for Quality 2
E Non-GMP examples in Pharmaceutical industry Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 2
K ANVISA B-GMP Auditing requirements for Contract Manufacturers Other Medical Device Regulations World-Wide 1
N Can a (class I) medical device be manufactured in a GMP certified site with no ISO13485? EU Medical Device Regulations 18
Q Need clarification on requirements.... Class i, gmp & 510(k) exempt Medical Device and FDA Regulations and Standards News 12
E South Korea, MFDS - GMP inspections Other Medical Device Regulations World-Wide 4
E MDSAP Audit - Our QMS conforms to ISO 13485:2016 and FDA GMP Canada Medical Device Regulations 9
A Any recommendation for ASQ's CPGP (Pharmaceutical GMP Professional) Certification exam questions? ASQ - American Society for Quality 2
W Interesting Discussion Class I, GMP Exempt and IEC62304 IEC 62304 - Medical Device Software Life Cycle Processes 2
J Brazil GMP license work with multiple BRH? Other Medical Device Regulations World-Wide 3
I GMP 21 CFR Part 11 Electronic Records Compliance Project Help Qualification and Validation (including 21 CFR Part 11) 9
W EU GMP Annex XI - What is an "appropriate QMS"? Other Medical Device Related Standards 2
S Compliance to Brazil GMP requirements Other Medical Device Regulations World-Wide 14
A Brazil - New RDC 183 - CBPF (GMP) question Other Medical Device Regulations World-Wide 6
L ISO 13485 and European GMP ISO 13485:2016 - Medical Device Quality Management Systems 3
I Moving into Clinical Trials and need to find GMP Suppliers 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
J Who can make a Correction of Entry on GMP Records Other Medical Device and Orthopedic Related Topics 1
S Traceability and the initiation of GMP Activities 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 6
A How do we implement a Process Approach ISO 13485:2016 - Existing GMP QMS Other ISO and International Standards and European Regulations 2
J KGMP (Korean GMP requirements) vs. ISO 13485 Other Medical Device Regulations World-Wide 8
R Network/Computer Data Migration Sampling GMP Software Quality Assurance 1
S Could the term "GMP" be used in a Medical Device world? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5

Similar threads

Top Bottom