Ready-to-use pre-processed by SteriPack
EU GMP Annex 1: Manufacture of Sterile Medicinal Products governing rules have been updated and come into force on 25 August 2023. One of the new rule requirements is associated with Contamination Control Strategy.
SteriPack offers the following services that are required prior to final aseptic preparations and processes:
- Comprehensive incoming inspection
- Post pre-processing inspection
- Sterilization management
Outsource your manufacturing processes by utilizing EU GMP Annex 1 compliant primary packaging components, i.e., caps, stoppers, syringe plungers.
SteriPack is a leading global contract manufacturer serving the pharmaceutical, medical device and diagnostic markets. Our global reach expands to more than 50 countries with manufacturing facilities strategically located across Europe, Asia, and North America, ensuring support for customers worldwide. Working under cGMP and ISO 13485, SteriPack provides the highest quality contract services:
- contract assembly and packaging for pharmaceutical and combination products
- design & development
- human factors
- final kitting
- serialization & aggregation
Founded over 25 years ago in Ireland, SteriPack was born from a desire to do it better. Better customer focus, better lead times, better manufacturing processes, better quality control, but most importantly a better approach to solving customer problems. Our mission from the outset has been clear ‘to be the number one pain reliever for the world’s largest OEM & Pharmaceutical companies’. When you’ve identified a manufacturing pain point within your organization the next step should be to outsource this pain and make it better through SteriPack. Doing it better commits SteriPack to continually partner with our clients to create value through enhanced solutions for quality, service, products and processes.