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Infographic: Performance Snapshot for 2023

January 17, 2024

INFOGRAPHIC:  A snapshot of how SeerPharma supported its clients with Quality and GMP Best-Practices in 2023 through QA & GMP Consulting, Auditing, Training and MasterControl "Qx" electronic Quality Management Systems (eQMS) & "Mx" Manufacturing Execution Systems (MES) with electronic Batch Records (eBR).

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Infographic: Performance Snapshot for 2022

January 12, 2023

INFOGRAPHIC:  A snapshot of how SeerPharma supported its customers with Quality and GMP Best-Practices in 2022.

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Infographic: Performance Snapshot for 2021

January 27, 2022

INFOGRAPHIC:  A snapshot of how SeerPharma supported its customers with Quality and GMP Best-Practices in 2021.

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Infographic: Performance Snapshot for 2020

January 12, 2021

INFOGRAPHIC:  A snapshot of how SeerPharma supported its customers with Quality and GMP Best-Practices in 2020.

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Virtual QA and GMP Consulting

April 06, 2020

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...

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Infographic: QA & GMP Compliance Performance Snapshot for 2019

January 08, 2020

INFOGRAPHIC:  A snapshot of how SeerPharma supported its clients in 2019 on matters of Quality Assurance and GMP compliance.

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Infographic: QA & GMP Compliance Performance Snapshot for 2017

January 03, 2018

INFOGRAPHIC:  A snapshot of how SeerPharma has supported its clients in 2017 on matters of QA and GMP compliance.

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Infographic: QA & GMP Compliance Performance Snapshot for 2016

March 02, 2017

INFOGRAPHIC:  A snapshot of how SeerPharma has supported its clients in 2016 on matters of QA and GMP compliance.

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CSV Gap Assessment for Pharmaceutical Distributor

November 15, 2016

A major pharmaceutical distribution organisation engaged the services of SeerPharma (Singapore) Pte Ltd to provide a review on the compliance of its core SAP-Centric solution to the GxP Computer Systems Validation (CSV) requirements of both FDA 21 CFR Part 11 and PIC/S Guide to GMP Annex 11. There were 2 phases to this project.

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Pharmaceutical Manufacturers Association Recommends G(QC)LP Services

September 05, 2016

One of our senior consultants in Singapore, received the following glowing recommendation from the Sri Lanka Pharmaceutical Manufacturers' Association (SLPMA) which is a testament to the quality of our team in Singapore who continually strive to deliver exceptional service to customers in the region.

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