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SeerPharma Blog

Automating Material Management

May 17, 2019

How SeerPharma worked closely with a leading Australian manufacturer in Tasmania to automate its material management processes.

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SeerPharma Partners with MasterControl

December 06, 2018

SeerPharma has over 25 years of experience implementing electronic Quality Management System (eQMS) solutions for companies operating in regulated environments. With extensive experience in the industry, we are excited to announce that we have now signed on to become a Partner for MasterControl.

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SeerPharma Presents on Quality Management System Certification

April 30, 2018

SeerPharma was invited by the Stevanato Group and Lonza to present on Pharmaceutical Quality Management System (QMS) Certification at The Innovative Solutions for Pharmaceutical Packaging Roadshow in Singapore.

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SeerPharma to Present on Quality Management System Certification

February 15, 2018

SeerPharma have been invited by the Stevanato Group and Lonza to present on Pharmaceutical Quality Management System Certification at The Innovative Solutions for Pharmaceutical Packaging Roadshow in Singapore.

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Electronic Quality Management System (eQMS) for Pharmaceutical Company

December 15, 2016

SeerPharma’s Software Solutions team has been engaged to implement an electronic Quality Management System (eQMS) for a major multinational pharmaceutical company.

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GMP Coaching Program Assists Biopharmaceutical Manufacturer

November 11, 2016

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.

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Pharmaceutical and Medical Device QMS Solutions

August 31, 2016

The SeerPharma team has been busy implementing electronic Quality Management Systems (eQMS) for a variety of companies ranging from pharmaceutical, nutraceutical, veterinary and medical device companies.

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Medical Device Company Engages SeerPharma for ISO 13485 QMS

June 15, 2016

 SeerPharma has assisted an Australian 3D Printing Medical Device company to develop an ISO 13485 compliant Quality Management System (QMS).

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Effective Corrective and Preventive Action (CAPA) for Medical Devices

June 09, 2016

As a Medical Device company, you are required to investigate the cause of quality failures or production problems. Surprisingly though, “Failure to thoroughly investigate…” is a common finding from quality (management) system inspections and audits against FDA 21 CFR Part 820 and ISO 13485.

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GMP Training and GMP Consulting on 3 Hot Topics from the ARCS Congress

May 13, 2015

The Quality / GMP stream hosted by ISPE at this year’s ARCS congress was a great opportunity to explore the latest issues and trends. Feedback and questions raised during the Quality / GMP sessions identified three current areas of interest to many involved in this area of work. Namely the approach and use of Quality Management Systems,...

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