SEETHARAM KANDARPA
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Tag: Inspection
MHRA implements new Software for risk based Inspection Planning
https://seetharamkandarpa.webnode.in/news/mhra-implements-new-software-for-risk-based-inspection-planning/
New EMA Inspection Requirements on Good Distribution Practices (GDP)
https://seetharamkandarpa.webnode.in/news/new-ema-inspection-requirements-on-good-distribution-practices-gdp-/
Denying, Delaying, And Refusing: How to Fail a FDA Inspection
https://seetharamkandarpa.webnode.in/news/denying-delaying-and-refusing-how-to-fail-a-fda-inspection/
FDA Inspection Reports: What are various results and their significance?
https://seetharamkandarpa.webnode.in/news/fda-inspection-reports-what-are-various-results-and-their-significance-/
FDA is proposing a regulation to implement administrative detention authority during inspections
https://seetharamkandarpa.webnode.in/news/fda-is-proposing-a-regulation-to-implement-administrative-detention-authority-during-inspections/
USFDA Draft Guidance - Circumstances that Constitute Delaying, Denying, Limiting, or Refusing a Drug Inspection
https://seetharamkandarpa.webnode.in/news/usfda-draft-guidance-circumstances-that-constitute-delaying-denying-limiting-or-refusing-a-drug-inspection/
More Inspections by USFDA in 2014
https://seetharamkandarpa.webnode.in/news/more-inspections-by-usfda-in-2014/
GCP and Bioequivalence Studies: new FDA/EMA Initiative
https://seetharamkandarpa.webnode.in/news/gcp-and-bioequivalence-studies-new-fda-ema-initiative/
GMP Inspections: Enhanced International Collaboration
https://seetharamkandarpa.webnode.in/news/gmp-inspections-enhanced-international-collaboration/
Personal overview of FDA Commissioner Margaret A. Hamburg about visit in India
https://seetharamkandarpa.webnode.in/news/personal-overview-of-fda-commissioner-margaret-a-hamburg-about-visit-in-india/
New Procedure for co-ordinating GCP-Inspections by CHMP
https://seetharamkandarpa.webnode.in/news/new-procedure-for-co-ordinating-gcp-inspections-by-chmp/
USFDA Inspections/483s Dashboard
https://seetharamkandarpa.webnode.in/news/usfda-inspections-483s-dashboard/
USFDA 483s Published in 2014 by USFDA
https://seetharamkandarpa.webnode.in/news/usfda-483s-published-in-2014-by-usfda/
Health Canada Launched New Drug and Product Inspections Database
https://seetharamkandarpa.webnode.in/news/health-canada-launched-new-drug-and-product-inspections-database/
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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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