I need an example GMP Manual

D

DzCoder

#1
#1
Hello everyone

Please I'm newbie in QA, and I'm looking for GMP Manual, I don't find it free, so any help are welcome

Cheers
:thanx:
 
Standard Work Instruction Software by Dozuki
Elsmar Forum Sponsor
D

dsanabria

Quite Involved in Discussions
#2
#2
First - What is GMP? - different industry have different interpretation of GMP.

Second - Did you looked into the "Free Files"? - small rectangular box on top of the main page. (below "THE ELSMAR COVE Discussion Forums)
 
Last edited by a moderator:
D

DzCoder

#3
#3
dsanabria said:
First - What is GMP? - different industry have different interpretation of GMP.

Second - Did you looked into the "Free Files"? - small rectangular box on top of the main page. (below "THE ELSMAR COVE Discussion Forums)
Click to expand...
I'm talking about GMP manual for phar-Prodection, look an this link u will see, gmp-manual(dot)com , there are what we call filelogi, this software regrouped any information about GPM and ...

Thank you
 
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
L I need an example rework procedure/instruction for injected plastic parts Document Control Systems, Procedures, Forms and Templates 2
O Need Example PFMEA for Turret Punch Press Manufacturing and Related Processes 2
L Need an example of an "FQCR" - A final quality control report. ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
M Need an example of QFD application in Automotive Industry Design and Development of Products and Processes 1
T New to ISO 14001 - Need example of Environmental Aspect/Impact for a HVAC Contractor ISO 14001:2015 Specific Discussions 3
S Need an example of Master Document Control Register ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
N Audit Summary Report - Need template example and help Internal Auditing 3
L Being audited on AS9100 30th July - need example flow chart AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 15
L AS9100B Quality System Manual: Need an example! Quality Management System (QMS) Manuals 7
A Safety Hazard Analysis Report - Need format or an example AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
W Drawing CUSUM Control Charts - Need a simple step by step example Quality Tools, Improvement and Analysis 3
C APQP Meeting Agenda - Need Example and How to keep the meetings focused & on track APQP and PPAP 7
E Successful Gage R&R Anova or X/R? Need example Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 6
T ISO 17025 Validation Procedure - Need Example ISO 17025 related Discussions 11
Crusader Spill Containment Procedure template - Need example Miscellaneous Environmental Standards and EMS Related Discussions 12
A Need Example of Metrics for Internal Audit Process. Internal Auditing 6
G I need an example of how to do a Control Plan with GM's GP-11 FMEA and Control Plans 3
O ISO 14001 Implementation Schedule - I need help and example schedule ISO 14001:2015 Specific Discussions 2
Q Need Example of Completed Process Identification Tool IATF 16949 - Automotive Quality Systems Standard 5
B Machining FMEA - I need help for good example FMEA and Control Plans 2
M Suppliers - Certified or compliant to ISO/QS etc. Need letter example Supplier Quality Assurance and other Supplier Issues 2
R What information do i need to get from the device manufacturer 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 0
S Need guidance on project ISO 13485:2016 - Medical Device Quality Management Systems 2
H Need MSA 4th ed. compliant attribute MSA template General Measurement Device and Calibration Topics 4
J Need Change Control Yes/No Decision Tree Template ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1
C Does an accessory need an IFU if it use is discussed in the Parent device IFU? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5
B Countries with no need for FSC (Free sales certificate) Other Medical Device Regulations World-Wide 0
R The term "Benefit Risk Ratio" in EU MDR, do I need to present benefit risk analysis as a RATIO Risk Management Principles and Generic Guidelines 4
A Brexit When does the UK responsible person need to be in place? UK Medical Device Regulations 10
R Do we need issue ECN (Engineering Change Notice) towards updated Material Specification? Design and Development of Products and Processes 2
N IPC-A-630 - Is this free or do i really need to pay for it? Manufacturing and Related Processes 3
C ISO/ IEC 17021 Resource requirement (need help) Document Control Systems, Procedures, Forms and Templates 5
P Need a programmer for QVI's VMS software for optical inspection machine Inspection, Prints (Drawings), Testing, Sampling and Related Topics 0
silentmonkey How to decide what characteristics need to be verified during incoming inspection? ISO 13485:2016 - Medical Device Quality Management Systems 5
D Change Approval Requirements - Does every change need formal customer approval? Design and Development of Products and Processes 17
T Do I need a qualified compiler for class B software? IEC 62304 - Medical Device Software Life Cycle Processes 3
E 13485:2016, Sections 4.1.6, 7.5.6 and 7.6 - Validation of Software - Need some Advice please ISO 13485:2016 - Medical Device Quality Management Systems 3
C ISO 13485 :2016 - CAPA - Does every CAPA need to be checked by regulations? ISO 13485:2016 - Medical Device Quality Management Systems 9
L Proof of Concept Studies - Do we need to comply with SAE reporting? Medical Device and FDA Regulations and Standards News 3
gunnyshore Adding a new facility - do I need to submit an amendment to the MDL or MDEL, or both? Canada Medical Device Regulations 3
N FDA UDI - Label vs. Labeling - Does the insert need to include UDI? Other US Medical Device Regulations 1
SocalSurfer AS9100 new certificate, but need QMS software, help Quality Assurance and Compliance Software Tools and Solutions 2
A Demonstration of Equivalence - Need for comparing biological characteristics for an SamD EU Medical Device Regulations 1
G Need to change KPI we called NC parts (maximum 3%.) to FTQ (first time quality) IATF 16949 - Automotive Quality Systems Standard 4
W Need for current design or process control FMEA and Control Plans 2
L Turkish Requirements - Does the Software need to be translated? CE Marking (Conformité Européene) / CB Scheme 2
J Need for a cleanroom in the manufacture of a medical device for a clinical trial EU Medical Device Regulations 4
S Need help with analysing a survey on minitab Using Minitab Software 1
M IATF 16949 8.5.1.3 Verification of job set-ups - Do we need secondary check? IATF 16949 - Automotive Quality Systems Standard 7
P Electrosurgical Device User Need: Cord Flexibility -> Requirement Other Medical Device and Orthopedic Related Topics 4

Similar threads

Top Bottom