Aseptic Filling Expertise

Publisher: Dec Group

Access this content

Your content has been opened.

Please verify you are a human before downloading this content.

Aseptic Filling Expertise has been emailed to . Entered the wrong email?

Don't see the content in your inbox?
Make sure to check your spam and other messages folders.

Can't get to your email right now?

To complete your registration and access this content, enter the sign-in code sent to your email.

Please enter a valid verification code.

Code sent to:

Also, remember to check in your spam, promotions, and other folders.


Register to access this content


By accessing content on the Pharmaceutical Manufacturing Resource Directory you agree to our Terms of Service and Privacy Policy; and, you acknowledge that your information may be shared with the content publisher.

Aseptic Filling Expertise

Technological developments in the pharmaceutical industry have advanced rapidly over the last decades. One field of particular interest has been aseptic and sterile primary packaging. Primary packaging of pharmaceutical products often involves filling containers (including vials, syringes and bottles) with powders and/ or liquid solutions. Manufacturing staff, equipment and premises are all subject to stringent quality controls – and for good reason: patient safety. In order to ensure the safety and quality of pharmaceutical products, every manufacturer in the pharmaceutical industry is compelled to adhere to the Good Manufacturing Practice (GMP) guidelines. Recently, a complete draft revisionI of Annex 1 (Manufacture of Sterile Medicinal Products) of the GMP has been released. This document intends to provide information on the latest status, trends and technologies in parenteral filling equipment.