SEETHARAM KANDARPA
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Tag: WHO
WHO publishes Draft on Revised Process Validation Guideline: Validation Life-Cycle Required
https://seetharamkandarpa.webnode.in/news/who-publishes-draft-on-revised-process-validation-guideline-validation-life-cycle-required/
WHO Guideline on Quality Risk Management finalised
https://seetharamkandarpa.webnode.in/news/who-guideline-on-quality-risk-management-finalised/
WHO publishes Variations Guideline for Prequalified APIs and Medicinal Products
https://seetharamkandarpa.webnode.in/news/who-publishes-variations-guideline-for-prequalified-apis-and-medicinal-products/
New WHO Initiative "Good Pharmacopoeial Practices"
https://seetharamkandarpa.webnode.in/news/new-who-initiative-good-pharmacopoeial-practices/
WHO revises Guideline for Maximum Hold Times
https://seetharamkandarpa.webnode.in/news/who-revises-guideline-for-maximum-hold-times/
WHO revises GMP Guide regarding the Principles of GMP
https://seetharamkandarpa.webnode.in/news/who-revises-gmp-guide-regarding-the-principles-of-gmp/
WHO publishes revised draft on GTDP for pharmaceutical starting material
https://seetharamkandarpa.webnode.in/news/who-publishes-revised-draft-on-gtdp-for-pharmaceutical-starting-material/
WHO published revised draft on the Guideline on "Hold Time" studies
https://seetharamkandarpa.webnode.in/news/who-published-revised-draft-on-the-guideline-on-hold-time-studies/
Draft on Process Validation by WHO
https://seetharamkandarpa.webnode.in/news/draft-on-process-validation-by-who/
Fake Antibiotics Feed Growing Worldwide Superbugs Threat
https://seetharamkandarpa.webnode.in/news/fake-antibiotics-feed-growing-worldwide-superbugs-threat/
WHO Called for Increased Transparency in Medical Research
https://seetharamkandarpa.webnode.in/news/who-called-for-increased-transparency-in-medical-research/
New WHO TRS 992 (May 2015) having guidance on Hold time study, Process validationand stirage & transport of products
https://seetharamkandarpa.webnode.in/news/new-who-trs-992-may-2015-having-guidance-on-hold-time-study-process-validationand-stirage-transport-of-products/
WHO Draft on 'SUPPLEMENTARY GUIDELINES ON GMP FOR HVAC SYSTEMS FOR NON-STERILE PHARMACEUTICAL DOSAGE FORMS'
https://seetharamkandarpa.webnode.in/news/who-draft-on-supplementary-guidelines-on-gmp-for-hvac-systems-for-non-sterile-pharmaceutical-dosage-forms/
cGMP Guidelines
https://seetharamkandarpa.webnode.in/products/product-1/
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About Me
SEETHARAM KANDARPA
Seetharam Kandarpa Receives ASQ-Certified Manager of Quality/Organizational Excellence
Web Series 2 of ASQ CQA Mentoring Class: Auditing Fundamentals on 30 July 2017
Overview of ASQ Certified Pharmaceutical GMP Professional (CPGP)
Web Series Session 1: Overview of ASQ Certified Quality Auditor conducted on 21 May 2017
Register to Join Mentoring Class for ASQ-CQA
Mentoring Class for ASQ-CQA
G.ONE (GMP-ONE)- One Spot for all GMP Links required in our JEEVAN
Seetharam Kandarpa Receives ASQ Quality Auditor
Seetharam Kandarpa Receives ASQ-Certified Pharmaceutical GMP Professional
ISO 9001: 2008 Quality Management Systems – Requirements
My new Mobile Application "SRK GCP World"
MACO Calculation Sheet in Cleaning Validation
My new Mobile Application "SRK GMP Videos"
"SRK CLEANING VALIDATION"- My new mobile application
"SRK GMP OCEAN"- My Mobile Application Works for Android & HTML5
"SRK GMP FAQ"- My new Mobile Application
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