Pharma & Awareness & Recreation Video

13/06/2022

https://pharmaguidances.com/jobs/jobs-in-vnai-hiring-freshers-apprenticeship-experienced-candidates-for-qc-rd-production-srp-engg-qa-ehs-fire-safety-department/

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22/12/2020

https://play.google.com/store/apps/details?id=com.alvinaalice.drugsformulations

21/12/2020

https://pharmaguidances.com/plastics-as-packaging-material/

PLASTICS AS PACKAGING MATERIAL Plastics in packaging have proved useful for a number of reasons, including the ease with which they can be formed, their high quality, and the freedom of design to which they can be changed. Plastic containers are extremely resistant to breakage and thus offer safety....

08/11/2020

https://pharmaguidances.com/cleaning-validation-glossary-of-terms/

Cleaning Validation Glossary of Terms 1 Acceptable daily intake An amount of a substance administered or consumed on a daily basis that will not produce a pharmacological or toxic response 2 Analyte Substance for which an analysis is being performed 3 API Active pharmaceutical ingredient ...

04/11/2020

https://pharmaguidances.com/general-principles-for-pharmaceutical-water-systems-as-per-who/

General principles for pharmaceutical water systems Pharmaceutical water production, storage and distribution systems should be designed, installed, commissioned, qualified and maintained to ensure the reliable production of water of an appropriate quality. It is necessary to validate the water prod...

04/11/2020

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03/11/2020

https://pharmaguidances.com/materials-in-pharmaceutical-as-per-who-guideline/

Materials in Pharmaceutical as per WHO Guideline Principle. The main objective of a pharmaceutical plant is to produce finished products for patients’ use from a combination of materials (starting and packaging). Materials include starting materials, packaging materials, gases, solvents, process a...

03/11/2020

https://pharmaguidances.com/guidance-document-cleaning-validation/

Guidance Document Cleaning Validation Scope Introduction Principles Validation of Cleaning Processes Equipment and Personnel Microbiological Considerations Documentation Analytical Methods Sampling, Rinsing, Rinse Samples and Detergents Establishment of Limits Change Control/revalid ...

03/11/2020

https://pharmaguidances.com/sop-on-sop/

SOP on SOP Objective : To lay down a procedure for the preparation, approval and control of Standard Operating Procedures. Scope: This Standard Operating Procedure is applicable for the preparation and implementation of all Standard Operating Procedures to be followed at Pharmaceutical Company. Resp...

30/10/2020

https://pharmaguidances.com/ich-q8-q9-q10-questions-and-answers/

ICH Q8/Q9/Q10 1.1 For General Clarification Date of Approval Questions Answers 1.0 June 2009 Is the minimal approach accepted by regulators? Yes. The minimal approach as defined in Q8(R2) (sometimes also called ‘baseline’ or ‘traditional’ approach) is the expectation that is to be achie ...