INFOGRAPHIC: A snapshot of how SeerPharma supported its customers with Quality and GMP Best-Practices in 2020.
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...
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...
INFOGRAPHIC: A snapshot of how SeerPharma supported its clients in 2019 on matters of Quality Assurance and GMP compliance.
Kalbe Farma is a leading healthcare provider in Indonesia, with extensive operations throughout the South East Asian region. Its’ subsidiary PT Kalbio Global Medika (KGM) has recently opened a new 11,000 square meter factory in Indonesia, which received a Honourable Mention for the 2017 Facility of the Year Awards from ISPE.
INFOGRAPHIC: A snapshot of how SeerPharma has supported its clients in 2017 on matters of QA and GMP compliance.
INFOGRAPHIC: A snapshot of how SeerPharma has supported its clients in 2016 on matters of QA and GMP compliance.
Cell therapies are an emerging form of healthcare that have started to produce transformative outcomes for patients with previously refractory diseases, but they are substantially more complex than small molecule or biologic drugs and present significant challenges for researchers and companies in cell therapy translation.
A biopharmaceutical manufacturer engaged SeerPharma to provide on-going coaching to their Quality personnel and advise on improvements to help prepare for a FDA inspection.
GMP Data Integrity is an issue that a number of our clients have approached us about recently. The concept of Data Integrity has been around for quite some time, with the TGA introducing the concept of electronic records in to the previous Australian code of GMP back in 1990, while the FDA made 21 CFR Part 11 Electronic records and signatures...
