Aesica Pharmaceuticals S.r.I. Implements Serialization System - Pharmaceutical Technology

Latest Issue
PharmTech

Latest Issue
PharmTech Europe

Aesica Pharmaceuticals S.r.I. Implements Serialization System

PTSM: Pharmaceutical Technology Sourcing and Management
Volume 10, Issue 7

Aesica Pharmaceuticals S.r.l. has announced the launch of a QAD integrated serialization system at its site in Pianezza to comply with change from China’s Food and Drug Administration (CFDA). The new requirements brought forward by CFDA cut the serialization implementation deadline to from 12 months to three months.

In partnership with QAD, a provider of enterprise software solutions, Aesica reports that the company implemented a solution that assured serialization compliance for two pharmaceutical products for the Chinese market.

The new requirements are designed to maintain customer safety, while fighting drug counterfeiting, streamlining the recall process, and minimizing financial loss. The project involved upgrading and utilizing a serialization module developed in QAD Enterprise Applications that allows Aesica Pharmaceuticals S.r.I. to identify individual packaging down to the smallest sellable unit sizes and aggregate individual unit serial numbers as packages are bundled, boxed and placed on shipping pallets. Aesica Pianezza can seamlessly track and trace each single pack of medication and report serial numbers to the required government agencies for a small number of products once they have been produced and imported.

Source: Aesica Pharmaceuticals

ADVERTISEMENT

blog comments powered by Disqus
LCGC E-mail Newsletters

Subscribe: Click to learn more about the newsletter
| Weekly
| Monthly
|Monthly
| Weekly

Survey
FDASIA was signed into law two years ago. Where has the most progress been made in implementation?
Reducing drug shortages
Breakthrough designations
Protecting the supply chain
Expedited reviews of drug submissions
More stakeholder involvement
Reducing drug shortages
70%
Breakthrough designations
4%
Protecting the supply chain
17%
Expedited reviews of drug submissions
2%
More stakeholder involvement
7%
View Results
Eric Langerr Outsourcing Outlook Eric LangerRelationship-building at Top of Mind for Clients
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerRisk Reduction Top Driver for Biopharmaceutical Raw Material Development
Jill Wechsler Regulatory Watch Jill Wechsler Changes and Challenges for Generic Drugs
Faiz Kermaini Industry Insider Faiz KermainiNo Signs of a Slowdown in Mergers
Ebola Outbreak Raises Ethical Issues
Better Comms Means a Fitter Future for Pharma, Part 2: Realizing the Benefits of Unified Communications
Better Comms Means a Fitter Future for Pharma, Part 1: Challenges and Changes
Sandoz Wins Biosimilar Filing Race
NIH Translational Research Partnership Yields Promising Therapy
Source: PTSM: Pharmaceutical Technology Sourcing and Management,
Click here