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

483

Home » 483 » Page 8

Design BMS (Building Management System) in Pharmaceuticals Industries

Posted by By Palash Das May 7, 2014Posted inAir Handling System, Validation
Read More

Selection of Glass Vial Sterile Injectable product

Posted by By Palash Das March 21, 2014Posted inDrug regulatory and guidelines, News Updates
Read More

Interview Questions for Pharmaceutical industry related jobs (QA,QC,Production,RA,f&d) for B.pharma /M.pharma (Part 6)

Posted by By Palash Das March 16, 2014Posted inInterview & Placement, Quality Assurance9 Comments
Read More

Qualifying Disinfection for Critical Environments and Cleanrooms

Posted by By Palash Das March 13, 2014Posted inQuality Assurance, Validation
Read More

Safety is 1st priority

Posted by By Palash Das March 6, 2014Posted inNews Updates, Quality Assurance
Read More

Start Clean Room Qualification

Posted by By Palash Das February 17, 2014Posted inQuality Assurance, Validation1 Comment
Read More

THE TEN GOLDEN RULES OF GMP

Posted by By Palash Das February 10, 2014Posted inNews Updates, Quality Assurance
Read More

Water System Design In Pharmaceutical Industry In Sterile Injectable Facility

Posted by By Palash Das February 5, 2014Posted inQuality Assurance, Validation
Read More

Equipment cleaning and use log as per regulatory requirment

Posted by By Palash Das December 31, 2013Posted inQuality Assurance, Validation
Read More

A to Z Risk Management with statistical approach

Posted by By Palash Das December 6, 2013Posted inNews Updates, QMS, Quality Assurance4 Comments
Read More

Posts pagination

Previous page 1 … 6 7 8 9 10 … 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