Skip to content
Pharmaceutical Resource & Education Services
  • Home
    • About US
  • Blog
  • Archives
    • DOC Library
    • Video Library
  • PRES CoP
  • Contact

483

Home » 483 » Page 6

Data Integrity (Part-III) (Some Major Observations)

Posted by By Palash Das December 23, 2015Posted inDrug regulatory and guidelines, QMS, Quality Assurance
Read More

Data Integrity Part-II (Laboratory)

Posted by By Palash Das December 22, 2015Posted inDrug regulatory and guidelines, QMS, Quality Assurance
Read More

Data Integrity -Part-I

Posted by By Palash Das December 22, 2015Posted inDrug regulatory and guidelines, QMS
Read More

Management of Corrective and Preventive Action (CA-PA)

Posted by By Palash Das November 30, 2015Posted inQMS, Quality Assurance
Read More

Discussion for establishment of risk based approach on airflow visualization in cleanrooms

Posted by By Palash Das November 21, 2015Posted inValidation
Read More

Popular methods of Risk Assessment (Part-II)

Posted by By Palash Das November 18, 2015Posted inQMS, Quality Assurance28 Comments
Read More

Popular methods of Risk Assessment (Part I)

Posted by By Palash Das November 17, 2015Posted inQMS, Quality Assurance
Read More

Label Control

Posted by By Palash Das November 2, 2015Posted inUncategorized
Read More

Where should airflow velocity measurements be taken, with respect to a filling line or other aseptic processing areas?

Posted by By Palash Das September 8, 2015Posted inValidation3 Comments
Read More

Application of near infrared spectroscopy to the analysis and fast quality assessment

Posted by By Palash Das June 25, 2015Posted infnd and production
Read More

Posts pagination

Previous page 1 … 4 5 6 7 8 … 13 Next page
Blog Archives
Recent Posts
  • EU Annex 1 compliance for superheated water steriliser – Part 2
  • EU Annex 1 compliance for superheated water steriliser – Part 1
  • Pre-Use Post-Sterilization Integrity Testing (PUPSIT): A Risk-Based Approach to Implementation
  • VHP Decontamination
  • Calculator for lethal rate (L) and F-physical (Fphys) values
Recent Comments
  • Narendra kulkarni on EU Annex 1 compliance for superheated water steriliser – Part 1
  • pro dentim on HOSTING REMOTE INSPECTION AT PHARMACEUTICAL FACILITIES
  • Personal finance blog on Get copy of 483’s, Non-compliance report and GMP certificate online from Agencies
  • Palash Das on How to Plan a Shutdown for Clean Room Air Handling Unit?
  • zoritoler imol on Trouble with Equilibration Time
Archives
Categories
Meta
  • Log in
  • Entries feed
  • Comments feed
  • WordPress.org

Subsribe To Our Newsletter

Stay in touch with us to get latest news and special offers.

Newsletter Signup Form

Address

1000, Brussels, Belgium

Email Us

mail2uscgmp@gmail.com

default-logo

Welcome to PRES. We are dedicated to provide technical solutions for sterile injectable business

Our Main Services

  • Mentoring
  • Business Analytics
  • Sterility Assurance
  • Validation Support
  • Audit Compliance

Follow Us

  • Facebook
  • Twitter
  • Youtube
  • Linkedin
Copyright © 2025 Pharmaceutical Resource & Education Services
Powered by Pharmaceutical Resource & Education Services
Scroll to Top