Презентация на тему «Good Practices in Production and Quality Control Related Guidelines»

Good Practices in Production and Quality Control

Related Guidelines John Startup

Good Practices in Production and Quality Control Related Guidelines

JOHN STARTUP

Training workshop: Training workshop on regulatory requirements for registration of Artemisinin based combined medicines and assessment of data submitted to regulatory authorities, February 23-27, 2009, Kampala, Uganda.

Basic Principles of GMP

Good Practices in Production and Quality Control. Related Guidelines

Basic Principles of GMP

The Ten Commandments of GMP

Section 16 and 17

Basic Principles of GMP

The Ten Commandments of GMP 1 Build Adequate Premises Equip Your Premises with plant and services fit for purpose. Maintain your premises and equipment Write procedures Validate your work/procedures

Section 16 and 17

Basic Principles of GMP

The Ten Commandments of GMP Train your workforce Record your work 8 Be clean in all things 9 Test for Quality 10 Audit for compliance.

Basic Principles of GMP

The WHO Guidelines EEC Guidelines(ORANGE GUIDE Eudralex Guidelines FDA Guidelines(CFR) MHRA Specific Topics

Basic Principles of GMP

Well documented and respected guidelines. Most available on the internet (OG is the exception)

Basic Principles of GMP

Do not forget EP, BP,USP Setting standards as opposed to guidelines

Basic Principles of GMP

PREMISES EEC 1.3 Specifically Annexe 1 Sterile Manufacture WHO Chapter 1 .12 HVAC Chapter 3 Sterile Manufacture. Eudralex Monograph

Basic Principles of GMP

EQUIPMENT EEC 3 and 5 (production) Specifically Annexe 1 Sterile Manufacture WHO Chapter 1 (includes HVAC) Chapter 3 Sterile Manufacture. Eudralex Guideline. Also Sterile Manufacture.

Basic Principles of GMP

CARE and MAINTENANCE EEC 3.34 to 3.44 Cleaning and maintenance. WHO 1.13 Company SOP for service schedule and pre programmed Maintenance (PPM)

Basic Principles of GMP

WRITE PROCEDURES Addressed in the Documentation chapters of the guidelines EEC 4.19 to 4.29 Include but not limited to Inventory control Sampling Testing and status control Manufacture and packaging Hygiene /environmental monitoring & control

Basic Principles of GMP

WRITE PROCEDURES Addressed in the Documentation chapters of the guidelines WHO 1.15 Eudralex PIC Annexe 13

Basic Principles of GMP

VALIDATION Validation protocols usually have a generic format # See WHO 1 appendix 6 Validation Master Plan PIC guideline 10063

Basic Principles of GMP

VALIDATION “A recorded protocol which demonstrates with a high degree of probability that any activity will repeatedly produce a result within a pre determined specification/requirement. ” All aspects of pharmaceutical manufacture require validation. Sufficiently important to be referred to throughout the guidelines. eg. WHO 1 appendix 6 Normally states the requirement (not negotiable) but rarely “how to”

Basic Principles of GMP

TRAINING WHO 1.10 and EEC 2.8 to 2.12 Detail training requirements General company culture On the job Outside courses Tests for proficiency Authorisation Training records

Basic Principles of GMP

RECORDS Found in the documentation chapters of the guidelines. Examples Analytical test records Batch manufacturing documents (BMR) Cleaning records

Basic Principles of GMP

CLEANLINESS AND HYGIENE Fleeting reference in EEC and WHO Guidelines PIC gives better information #

Basic Principles of GMP

QUALITY Quality Assurance Both OG and WHO describe in detail the elements of a robust quality system. Emphasises its all embracing function

Basic Principles of GMP

QUALITY Quality Control Quality control of raw materials Components Intermediates and finished products. Microbiology

Basic Principles of GMP

QUALITY Quality Control WHO 1.17 EEC 12.6 Quality control of raw materials Components Intermediates and finished products. Microbiology $ #

Basic Principles of GMP

AUDITING FOR COMPLIANCE WHO 1.8 EEC2.9 Describes the procedures Aspects of pharmaceutical production to be assessed. Includes audits of suppliers.

So what else is there

???

Basic Principles of GMP

ISO9000

GAMP

HTM 2010 Validation of Autoclaves BS 6001

Basic Principles of GMP

OTHERS ISPE Publications on good Pharma Practice HTM 2010 Validation of Autoclaves

Basic Principles of GMP

WHAT ELSE IS THERE Contract manufacture. Technical agreements. WHO 1.7 EEC 2.7 Both define contract giver and acceptor And their individual and shared responsibilities

Basic Principles of GMP

WHAT ELSE IS THERE Complaints Recalls Returns Stability programmes.

Basic Principles of GMP

All the guidelines presented are objectives which are not negotiable Nowhere does it say if it costs too much one can ignore the guideline Nowhere does it say if the resources are unavailable the guideline can be ignored. Whist not negotiable, the means /ways of achieving the objectives are a matter of company style” one man’s solution is another man’s disaster.