The Corrective and Preventative Action (CAPA) system is central to every Quality Management System (QMS). Quality professionals know the importance of managing CAPAs when a quality event occurs.
In the Pharmaceutical and Medical Device industries, document control is an essential quality system element and a regulated requirement because written instructions directly affect processes that impact product quality.
Virtual QA and GMP Consulting
For over 30 years SeerPharma has aided Pharmaceutical and Medical Device companies on matters of Quality Assurance and GMP compliance.
The current COVID-19 pandemic is seeing day to day quality related business operations challenged by attempting to deal with multiple personnel across different departments remotely. The need for immediate and...
This article was originally published by SeerPharma's business partner MasterControl and is republished here with their permission.
Digital transformation efforts are accelerating in a variety of manufacturing areas, with upwards of 73% of recently surveyed manufacturers saying they plan to increase their investment in smart factory technology...
In the Pharmaceutical and Medical Device industries, employees can affect product quality so they must be trained and assessed on a variety of documents (policies, SOPs etc.) and tasks relevant to their job role . As a Training Manager your paper-based system requires you to distribute training materials, tasks, reminders and tests in person or...
Introduction to Bioprocessing Course Postponed
The University of Technology Sydney (UTS) has scheduled postponed the first "Introduction to Bioprocessing" training session in the new 430m2 Biologics Innovation Facility (BIF) with its cGMP designed clean rooms and containment laboratories.
SeerPharma is excited to welcome the 2020 cohort of students who will embark on achieving Postgraduate Qualifications in Good Manufacturing Practice (GMP) from the University of Technology Sydney. The cohort represent a mix of graduates and working professionals from around the world, some of whom will undertake these studies on-campus in Sydney,...
SeerPharma to Deliver Bioprocessing Training Programs at UTS
The University of Technology Sydney (UTS) recently opened its Biologics Innovation Facility (BIF). The 430 square meter facility houses a series of clean rooms and containment laboratories meeting cGMP codes. The facility has been set up to provide the biotech and pharmaceutical sector with an opportunity to have their employees locally trained...
SeerPharma to Sponsor 8th Annual BioMelbourne Device + Diagnostics Lab
SeerPharma is excited to be sponsoring BioMelbourne Network’s 8th Annual Device + Diagnostics Lab, to be held on Thursday the 5th of March.
How Cloud Migration Has Become More Seamless for Regulated Companies
This article was originally published by SeerPharma's business partner MasterControl and is republished in-part here with their permission.