Pharma Industry Guidelines Validation

Validation of New Process

PharmaState Blog

-

25/06/2019

Process validation is the collection and evaluation of data, from the process design stage throughout production, which establishes scientific evidence that a process is capable of consistently delivering quality products.

FC-Validation Download

Related

PharmaState Blog

This is a platform for people working in the pharmaceuticals industry for Discussions, Jobs, News updates, Professional Profile display space and company business pages. PharmaState DNA is having four pillars: Quality, Transparency, Innovation & Benchmarks.

Share this article

Recent posts

Popular categories

Pharma Industry Guidelines316 Quality Assurance137 SOPs96 Production73 Quality Control72

Previous articleUSFDA: List of Off-Patent, Off-Exclusivity Drugs without an Approved Generic

Next articleAnalytical Method Transfer (AMT)

Leave a Reply Cancel reply

Recent comments

Harinder Yadav on SOP FOR OPERATION AND CLEANING OF COATING PAN

Tammie Houston on Bacteriology: Specimen Collection, Transport & Processing

Rahul Chaudhary on SOP for User Requirement Specification in Pharmaceutical Industry

Supratim Bhattacharjee on Online Pharmacies: Sweet or Bitter Pill?

Manufacturing ERP on Quality Assurance

PharmaState Blog on Pharma Brand Manager – A lucrative career choice

Abhinav Dongre on Pharma Brand Manager – A lucrative career choice

Trevor Keller on HVAC DESIGN FOR PHARMACEUTICAL FACILITIES

Business Alnavedic on History of Indian Pharma Industry

Ahmed Mohamed Elkhodragy on MACO Calculation

Mark Asare-Bediako on Cleaning Validation in Pharmaceutical Industry

Harish kumar kaim on SOP ON SOP (HOW TO PREPARE SOP) – PHARMACEUTICAL INDUSTRY

Ramdas Pol on SOP FOR POLARIMETER: OPERATION AND CALIBRATION

Jennifer Osunde on DEFECTS IN UNCOATED TABLETS

My Heart Doctormyheartdoctor on Healthy Culture at Workplace

Ram Kishor mandal on मेडिकल रिप्रेजेंटेटिव – एक शानदार करियर ऑप्शन क्यों है?

Laafon Galaxy on SOP FOR OPERATION AND CALIBRATION OF DIGITAL AUTOMATIC KARL FISCHER (KF) TITRATOR

sixphotosnuff on INDUCTION OF MEDICAL REPRESENTATIVES- From Day 1 to Day 5

rohit on HVAC DESIGN FOR PHARMACEUTICAL FACILITIES

keerthivasan on COMPLIANCE: KEY TO BUSINESS REPUTATION

Harry Kochat on Test Your Pharma Knowledge Part 1

Vinod on DEVIATION

Nageshwar on PASSIVATION PROCESS USED IN WATER SYSTEMS IN PHARMA INDUSTRY

RAGHUVEER SINGH YADAV on ABCDE of Intelligence for Professional Growth

Pritiksha Raj on Pharmaceutical Industry – Filling the Skill Gap

Ramesh Patel on SOP FOR OPERATION AND CLEANING OF HOMOGENIZER

Erawat on Quality Inspections

Pooja Dhiman on All about Pharm. D Course status in India

Sunil Kumar M on SITE ACCEPTANCE TEST (SAT)

pharmabeginers on SOP FOR CLEANING AND SANITIZATION OF DRAIN TRAPS

Khalid on IQ Protocol

Khalid on IQ Protocol

Yatherm Scientific on Procedure for Cleaning and Monitoring of Clean Room Pass Boxes

william maina on SOP on Handling Out Of Trend (OOT) Results

pradeep852 on SOP for Quality Management System (Documentation) in Pharmaceutical Industry

drpremrgoel1947 on SOP on Calibration of Weighing Balance

boiporitto on METAL DETECTOR TYPES AND USES IN PHARMA INDUSTRY

namrata banerjee on COMPLIANCE: KEY TO BUSINESS REPUTATION

namrata banerjee on COMPLIANCE: KEY TO BUSINESS REPUTATION

Bharat Ramani on COMPLIANCE: KEY TO BUSINESS REPUTATION

Kajal Bhattacharjee on COMPLIANCE: KEY TO BUSINESS REPUTATION

Nagabooshanam on Calibration of Reactor

PharmaState Blog on SOP for Sampling

PART -2 Quality Agreements | PharmaState Blog on Quality Agreements – PART 1

PART -1 Quality Agreements- What is it? | PharmaState Blog on Quality Agreements – PART 2

Ganga prasad on Qualification: V- Model Approach, Qualification Matrix, Qualification Activity

Gangaprasad on SOP – Planned Modification

Sujata Patel on SUGAM Portal, an e-Governance solution for CDSCO

Adharsha D on SOP FOR POLARIMETER: OPERATION AND CALIBRATION

Adharsha D on SOP FOR DETERMINATION OF SHELF LIFE OF SOLUTION IN LABORATORY

Ganga prasad on SOP for Quality Management System (Documentation) in Pharmaceutical Industry

MEXCONTROL on STABILITY STUDY PROTOCOL TEMPLATE – Pharmaceutical Industry

Jitendra Patel on SOP for User Requirement Specification in Pharmaceutical Industry

makcleanair2018 on Cleanroom Standards – ISO Guidelines

Jitendra Patel on SOP for Microbiological Analysis of Water

SOP on data integrity in Pharmaceutical Industry — PharmaState Blog – Pramod Sharma on SOP on Data Integrity in Pharmaceutical Industry

PharmaState Blog on Most frequently asked Pharma Regulatory Affairs Interview Q & A – Let’s ace the interview

Dr Appaji PV on Most frequently asked Pharma Regulatory Affairs Interview Q & A – Let’s ace the interview

Dr Appaji PV on Indian Pharmaceutical Industry: Statistics we should know

PharmaState Blog on Quiz on Janaushadhi Scheme – Pradhan Mantri Bhartiya Janaushadhi Pariyojana (PMBJP)

Dr Appaji PV on Quiz on Janaushadhi Scheme – Pradhan Mantri Bhartiya Janaushadhi Pariyojana (PMBJP)

Criteria for Selection of Clean Room Garments in Pharmaceuticals | PharmaState Blog on HVAC DESIGN FOR PHARMACEUTICAL FACILITIES

Bhavyasree Ravikrindi on SOP FOR OPERATION AND CLEANING OF HOMOGENIZER

Hatice on QUALIFICATION OF AUTOCLAVE

China’s Environmental Policies Impact on Indian Pharma Industry – PharmaState Blog on India, China & Pharma Industry: Current Scenario

Prasad on FROM ALCOA TO ALCOA PLUS- DATA INTEGRITY

Dheeraj on India, China & Pharma Industry: Current Scenario

Global employment data of Pharmaceutical Industry – PharmaState Blog – Best Job Hub on Global employment data of Pharmaceutical Industry

Prafull on Largest Pharma Companies in India as of March,2018 (based on Branded Generic Sales in India)

溫柔生產 on QUALIFICATION OF TUNNEL STERILIZING MACHINE

PIC/S [Pharmaceutical Inspection Convention and Pharmaceutical Inspection Scheme] – PharmaState Blog on PIC/S [Pharmaceutical Inspection Convention and Pharmaceutical Inspection Scheme]- Guidelines & Links

[SCHEDULE – M] SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL SOLID DOSAGE FORMS (TABLETS AND CAPSULES), PART I-B – PharmaState Blog on GOOD MANUFACTURING PRACTICES AND REQUIREMENTS OF PREMISES, PLANT AND EQUIPMENT FOR PHARMACEUTICAL PRODUCTS

[SCHEDULE – M] SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL SOLID DOSAGE FORMS (TABLETS AND CAPSULES), PART I-B – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF STERILE PRODUCTS, PARENTERAL PREPARATIONS (SMALL VOLUME INJECTABLES & LARGE VOLUME PARENTERALS) AND STERILE OPHTHALMIC PREPARATIONS

[SCHEDULE – M] SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL SOLID DOSAGE FORMS (TABLETS AND CAPSULES), PART I-B – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL LIQUIDS (SYRUPS, ELIXIRS, EMULSIONS AND SUSPENSIONS)

[SCHEDULE – M] SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL SOLID DOSAGE FORMS (TABLETS AND CAPSULES), PART I-B – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF TOPICAL PRODUCTS

[SCHEDULE – M] SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL SOLID DOSAGE FORMS (TABLETS AND CAPSULES), PART I-B – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF METERED-DOSE-INHALERS(MDI)

[SCHEDULE – M] SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL SOLID DOSAGE FORMS (TABLETS AND CAPSULES), PART I-B – PharmaState Blog on SPECIFIC REQUIREMENTS OF PREMISES, PLANT AND MATERIALS FOR MANUFACTURE OF ACTIVE PHARMACEUTICAL INGREDIENTS (BULK DRUGS)

[SCHEDULE – M] SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL SOLID DOSAGE FORMS (TABLETS AND CAPSULES), PART I-B – PharmaState Blog on REQUIREMENTS OF PLANT AND EQUIPMENT – PART-II

[SCHEDULE – M] SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL SOLID DOSAGE FORMS (TABLETS AND CAPSULES), PART I-B – PharmaState Blog on SCHEDULE M-I

[SCHEDULE – M] SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL SOLID DOSAGE FORMS (TABLETS AND CAPSULES), PART I-B – PharmaState Blog on REQUIREMENT OF FACTORY PREMISES FOR MANUFACTURE OF COSMETICS.

[SCHEDULE – M] SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL SOLID DOSAGE FORMS (TABLETS AND CAPSULES), PART I-B – PharmaState Blog on REQUIREMENTS OF FACTORY PREMISES FOR MANUFACTURE OF MEDICAL DEVICES

[SCHEDULE M] SPECIFIC REQUIREMENTS FOR MANUFACTURE OF STERILE PRODUCTS, PARENTERAL PREPARATIONS (SMALL VOLUME INJECTABLES & LARGE VOLUME PARENTERALS) AND STERILE OPHTHALMIC PREPARATIONS,PART – 1 A – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL SOLID DOSAGE FORMS (TABLETS AND CAPSULES)

[SCHEDULE M] SPECIFIC REQUIREMENTS FOR MANUFACTURE OF STERILE PRODUCTS, PARENTERAL PREPARATIONS (SMALL VOLUME INJECTABLES & LARGE VOLUME PARENTERALS) AND STERILE OPHTHALMIC PREPARATIONS,PART – 1 A – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL LIQUIDS (SYRUPS, ELIXIRS, EMULSIONS AND SUSPENSIONS)

[SCHEDULE M] SPECIFIC REQUIREMENTS FOR MANUFACTURE OF STERILE PRODUCTS, PARENTERAL PREPARATIONS (SMALL VOLUME INJECTABLES & LARGE VOLUME PARENTERALS) AND STERILE OPHTHALMIC PREPARATIONS,PART – 1 A – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF TOPICAL PRODUCTS

[SCHEDULE M] SPECIFIC REQUIREMENTS FOR MANUFACTURE OF STERILE PRODUCTS, PARENTERAL PREPARATIONS (SMALL VOLUME INJECTABLES & LARGE VOLUME PARENTERALS) AND STERILE OPHTHALMIC PREPARATIONS,PART – 1 A – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF METERED-DOSE-INHALERS(MDI)

[SCHEDULE M] SPECIFIC REQUIREMENTS FOR MANUFACTURE OF STERILE PRODUCTS, PARENTERAL PREPARATIONS (SMALL VOLUME INJECTABLES & LARGE VOLUME PARENTERALS) AND STERILE OPHTHALMIC PREPARATIONS,PART – 1 A – PharmaState Blog on SPECIFIC REQUIREMENTS OF PREMISES, PLANT AND MATERIALS FOR MANUFACTURE OF ACTIVE PHARMACEUTICAL INGREDIENTS (BULK DRUGS)

[SCHEDULE M] SPECIFIC REQUIREMENTS FOR MANUFACTURE OF STERILE PRODUCTS, PARENTERAL PREPARATIONS (SMALL VOLUME INJECTABLES & LARGE VOLUME PARENTERALS) AND STERILE OPHTHALMIC PREPARATIONS,PART – 1 A – PharmaState Blog on REQUIREMENTS OF PLANT AND EQUIPMENT – PART-II

[SCHEDULE M] SPECIFIC REQUIREMENTS FOR MANUFACTURE OF STERILE PRODUCTS, PARENTERAL PREPARATIONS (SMALL VOLUME INJECTABLES & LARGE VOLUME PARENTERALS) AND STERILE OPHTHALMIC PREPARATIONS,PART – 1 A – PharmaState Blog on SCHEDULE M-I

[SCHEDULE M] SPECIFIC REQUIREMENTS FOR MANUFACTURE OF STERILE PRODUCTS, PARENTERAL PREPARATIONS (SMALL VOLUME INJECTABLES & LARGE VOLUME PARENTERALS) AND STERILE OPHTHALMIC PREPARATIONS,PART – 1 A – PharmaState Blog on REQUIREMENT OF FACTORY PREMISES FOR MANUFACTURE OF COSMETICS.

[SCHEDULE M] SPECIFIC REQUIREMENTS FOR MANUFACTURE OF STERILE PRODUCTS, PARENTERAL PREPARATIONS (SMALL VOLUME INJECTABLES & LARGE VOLUME PARENTERALS) AND STERILE OPHTHALMIC PREPARATIONS,PART – 1 A – PharmaState Blog on REQUIREMENTS OF FACTORY PREMISES FOR MANUFACTURE OF MEDICAL DEVICES

[SCHEDULE M] GOOD MANUFACTURING PRACTICES AND REQUIREMENTS OF PREMISES, PLANT AND EQUIPMENT FOR PHARMACEUTICAL PRODUCTS, PART 1 – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL SOLID DOSAGE FORMS (TABLETS AND CAPSULES)

[SCHEDULE M] GOOD MANUFACTURING PRACTICES AND REQUIREMENTS OF PREMISES, PLANT AND EQUIPMENT FOR PHARMACEUTICAL PRODUCTS, PART 1 – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL LIQUIDS (SYRUPS, ELIXIRS, EMULSIONS AND SUSPENSIONS)

[SCHEDULE M] GOOD MANUFACTURING PRACTICES AND REQUIREMENTS OF PREMISES, PLANT AND EQUIPMENT FOR PHARMACEUTICAL PRODUCTS, PART 1 – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF TOPICAL PRODUCTS

[SCHEDULE M] GOOD MANUFACTURING PRACTICES AND REQUIREMENTS OF PREMISES, PLANT AND EQUIPMENT FOR PHARMACEUTICAL PRODUCTS, PART 1 – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF METERED-DOSE-INHALERS(MDI)

[SCHEDULE M] GOOD MANUFACTURING PRACTICES AND REQUIREMENTS OF PREMISES, PLANT AND EQUIPMENT FOR PHARMACEUTICAL PRODUCTS, PART 1 – PharmaState Blog on SPECIFIC REQUIREMENTS OF PREMISES, PLANT AND MATERIALS FOR MANUFACTURE OF ACTIVE PHARMACEUTICAL INGREDIENTS (BULK DRUGS)

[SCHEDULE M] GOOD MANUFACTURING PRACTICES AND REQUIREMENTS OF PREMISES, PLANT AND EQUIPMENT FOR PHARMACEUTICAL PRODUCTS, PART 1 – PharmaState Blog on REQUIREMENTS OF PLANT AND EQUIPMENT – PART-II

[SCHEDULE M] GOOD MANUFACTURING PRACTICES AND REQUIREMENTS OF PREMISES, PLANT AND EQUIPMENT FOR PHARMACEUTICAL PRODUCTS, PART 1 – PharmaState Blog on SCHEDULE M-I

[SCHEDULE M] GOOD MANUFACTURING PRACTICES AND REQUIREMENTS OF PREMISES, PLANT AND EQUIPMENT FOR PHARMACEUTICAL PRODUCTS, PART 1 – PharmaState Blog on REQUIREMENT OF FACTORY PREMISES FOR MANUFACTURE OF COSMETICS.

[SCHEDULE M] GOOD MANUFACTURING PRACTICES AND REQUIREMENTS OF PREMISES, PLANT AND EQUIPMENT FOR PHARMACEUTICAL PRODUCTS, PART 1 – PharmaState Blog on REQUIREMENTS OF FACTORY PREMISES FOR MANUFACTURE OF MEDICAL DEVICES

SCHEDULE M-I – PharmaState Blog on GOOD MANUFACTURING PRACTICES AND REQUIREMENTS OF PREMISES, PLANT AND EQUIPMENT FOR PHARMACEUTICAL PRODUCTS

SCHEDULE M-I – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF STERILE PRODUCTS, PARENTERAL PREPARATIONS (SMALL VOLUME INJECTABLES & LARGE VOLUME PARENTERALS) AND STERILE OPHTHALMIC PREPARATIONS

SCHEDULE M-I – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL SOLID DOSAGE FORMS (TABLETS AND CAPSULES)

SCHEDULE M-I – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL LIQUIDS (SYRUPS, ELIXIRS, EMULSIONS AND SUSPENSIONS)

SCHEDULE M-I – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF TOPICAL PRODUCTS

SCHEDULE M-I – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF METERED-DOSE-INHALERS(MDI)

SCHEDULE M-I – PharmaState Blog on SPECIFIC REQUIREMENTS OF PREMISES, PLANT AND MATERIALS FOR MANUFACTURE OF ACTIVE PHARMACEUTICAL INGREDIENTS (BULK DRUGS)

SCHEDULE M-I – PharmaState Blog on REQUIREMENTS OF PLANT AND EQUIPMENT – PART-II

SCHEDULE M-I – PharmaState Blog on REQUIREMENT OF FACTORY PREMISES FOR MANUFACTURE OF COSMETICS.

SCHEDULE M-I – PharmaState Blog on REQUIREMENTS OF FACTORY PREMISES FOR MANUFACTURE OF MEDICAL DEVICES

[SCHEDULE M-II] REQUIREMENT OF FACTORY PREMISES FOR MANUFACTURE OF COSMETICS. – PharmaState Blog on GOOD MANUFACTURING PRACTICES AND REQUIREMENTS OF PREMISES, PLANT AND EQUIPMENT FOR PHARMACEUTICAL PRODUCTS

[SCHEDULE M-II] REQUIREMENT OF FACTORY PREMISES FOR MANUFACTURE OF COSMETICS. – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF STERILE PRODUCTS, PARENTERAL PREPARATIONS (SMALL VOLUME INJECTABLES & LARGE VOLUME PARENTERALS) AND STERILE OPHTHALMIC PREPARATIONS

[SCHEDULE M-II] REQUIREMENT OF FACTORY PREMISES FOR MANUFACTURE OF COSMETICS. – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL SOLID DOSAGE FORMS (TABLETS AND CAPSULES)

[SCHEDULE M-II] REQUIREMENT OF FACTORY PREMISES FOR MANUFACTURE OF COSMETICS. – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL LIQUIDS (SYRUPS, ELIXIRS, EMULSIONS AND SUSPENSIONS)

[SCHEDULE M-II] REQUIREMENT OF FACTORY PREMISES FOR MANUFACTURE OF COSMETICS. – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF TOPICAL PRODUCTS

[SCHEDULE M-II] REQUIREMENT OF FACTORY PREMISES FOR MANUFACTURE OF COSMETICS. – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF METERED-DOSE-INHALERS(MDI)

[SCHEDULE M-II] REQUIREMENT OF FACTORY PREMISES FOR MANUFACTURE OF COSMETICS. – PharmaState Blog on SPECIFIC REQUIREMENTS OF PREMISES, PLANT AND MATERIALS FOR MANUFACTURE OF ACTIVE PHARMACEUTICAL INGREDIENTS (BULK DRUGS)

[SCHEDULE M-II] REQUIREMENT OF FACTORY PREMISES FOR MANUFACTURE OF COSMETICS. – PharmaState Blog on REQUIREMENTS OF PLANT AND EQUIPMENT – PART-II

[SCHEDULE M-II] REQUIREMENT OF FACTORY PREMISES FOR MANUFACTURE OF COSMETICS. – PharmaState Blog on SCHEDULE M-I

[SCHEDULE M-II] REQUIREMENT OF FACTORY PREMISES FOR MANUFACTURE OF COSMETICS. – PharmaState Blog on REQUIREMENTS OF FACTORY PREMISES FOR MANUFACTURE OF MEDICAL DEVICES

[ SCHEDULE M-III ] REQUIREMENTS OF FACTORY PREMISES FOR MANUFACTURE OF MEDICAL DEVICES – PharmaState Blog on GOOD MANUFACTURING PRACTICES AND REQUIREMENTS OF PREMISES, PLANT AND EQUIPMENT FOR PHARMACEUTICAL PRODUCTS

[ SCHEDULE M-III ] REQUIREMENTS OF FACTORY PREMISES FOR MANUFACTURE OF MEDICAL DEVICES – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF STERILE PRODUCTS, PARENTERAL PREPARATIONS (SMALL VOLUME INJECTABLES & LARGE VOLUME PARENTERALS) AND STERILE OPHTHALMIC PREPARATIONS

[ SCHEDULE M-III ] REQUIREMENTS OF FACTORY PREMISES FOR MANUFACTURE OF MEDICAL DEVICES – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL SOLID DOSAGE FORMS (TABLETS AND CAPSULES)

[ SCHEDULE M-III ] REQUIREMENTS OF FACTORY PREMISES FOR MANUFACTURE OF MEDICAL DEVICES – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF ORAL LIQUIDS (SYRUPS, ELIXIRS, EMULSIONS AND SUSPENSIONS)

[ SCHEDULE M-III ] REQUIREMENTS OF FACTORY PREMISES FOR MANUFACTURE OF MEDICAL DEVICES – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF TOPICAL PRODUCTS

[ SCHEDULE M-III ] REQUIREMENTS OF FACTORY PREMISES FOR MANUFACTURE OF MEDICAL DEVICES – PharmaState Blog on SPECIFIC REQUIREMENTS FOR MANUFACTURE OF METERED-DOSE-INHALERS(MDI)

[ SCHEDULE M-III ] REQUIREMENTS OF FACTORY PREMISES FOR MANUFACTURE OF MEDICAL DEVICES – PharmaState Blog on SPECIFIC REQUIREMENTS OF PREMISES, PLANT AND MATERIALS FOR MANUFACTURE OF ACTIVE PHARMACEUTICAL INGREDIENTS (BULK DRUGS)

[ SCHEDULE M-III ] REQUIREMENTS OF FACTORY PREMISES FOR MANUFACTURE OF MEDICAL DEVICES – PharmaState Blog on REQUIREMENTS OF PLANT AND EQUIPMENT – PART-II

[ SCHEDULE M-III ] REQUIREMENTS OF FACTORY PREMISES FOR MANUFACTURE OF MEDICAL DEVICES – PharmaState Blog on SCHEDULE M-I

[ SCHEDULE M-III ] REQUIREMENTS OF FACTORY PREMISES FOR MANUFACTURE OF MEDICAL DEVICES – PharmaState Blog on REQUIREMENT OF FACTORY PREMISES FOR MANUFACTURE OF COSMETICS.

Swetha on HVAC DESIGN FOR PHARMACEUTICAL FACILITIES

Faheemur Rahaman Khan on SOP FOR CLEANING PROCEDURE OF GENERAL MICROBIOLOGICAL TESTING AREA 3

Yolanda Allen on METAL DETECTOR TYPES AND USES IN PHARMA INDUSTRY

Swapnil Khodake on TOOLING FOR TABLETING

Alex on IND, NDA AND ANDA DRUG EVOLUTION PROCESS

Alex on QUALITY BY DESIGN (QBD)

Alex on QUALITY BY DESIGN (QBD)

Related

%d bloggers like this: