An Inspector’s View on Document and Batch Record Management
Virtual Lunch and Learn With SeerPharma and MasterControl
15 December 2021 | 12:00 – 1:00 p.m. AEDT
As a manufacturer, you know the important role documentation plays in good manufacturing practices. Goods that aren’t fully and properly documented can’t be released into a regulated market. And manufacturing sites cannot receive licences or certifications without a complete set of controlled documents. If you want to stay compliant and competitive, having the best possible practices for managing your documents and batch records is an absolute must.
While documentation requirements have been around for decades, the way companies navigate those requirements have changed. Whether it’s the role new technology can play in managing documentation or increased regulatory expectations, it’s more important than ever for your organisation to be aware of changes in the market and how to adapt to them.
SeerPharma has partnered with MasterControl for a virtual event designed to help you simplify documentation and improve good manufacturing practices at your business. Presented by SeerPharma's Andrew Giles (Partner), this presentation will draw from Andrew's 30+ years of pharmaceutical experience and history as a GMP inspector to give you an inside view on what your business should be doing in its document and batch record management.
Topics will include:
- The evolution of documentation in therapeutic goods.
- The challenges you can expect when adopting new technology.
- How to ensure compliance to changing regulatory expectations.
- How to improve good manufacturing practices at your business.
