In the medical device industry, internal audits are often viewed primarily as a regulatory requirement. ISO 13485:2016 requires organisations to assess the effectiveness of their Quality Management System (QMS). However, organisations that treat internal auditing purely as a compliance exercise risk missing a significant opportunity.
The future of quality management is no longer about forcing processes into rigid systems; it is about empowering organisations to design quality around their unique needs. That’s exactly where MasterControl’s Advanced Quality Event Management (AQEM) comes in.
INFOGRAPHIC: A snapshot of how SeerPharma supported its customers with Quality and GMP Best-Practices in 2025 by providing QA & GMP Consulting, Auditing & Training services as well as MasterControl solutions "Qx" electronic Quality Management Systems (eQMS) & "Mx" Manufacturing Execution Systems (MES) with electronic Batch Records (eBR).
For more than 35 years, SeerPharma has been a trusted partner to pharmaceutical and medical device organisations across the Asia-Pacific (APAC) region, providing expert guidance on Quality Management Systems (QMS) and Good Manufacturing Practice (GMP) compliance.
At the heart of our work lies a team of highly experienced quality and regulatory...
Life sciences organisations work across diverse countries, languages, and regulations, where accurate communication is vital for compliance and safety. Traditional translation methods are slow and error-prone, creating barriers to global alignment. MasterControl’s AI-powered eQMS removes these challenges by enabling instant translation, clear...
In this actionable webinar for quality leaders, we’ll reveal essential automation strategies and how to configure CAPA processes to match your unique business processes—without custom coding or IT dependencies. Learn how forward-thinking companies are leveraging configurable quality event management systems to dramatically reduce CAPA resolution...
INFOGRAPHIC: A snapshot of how SeerPharma supported its customers with Quality and GMP Best-Practices in 2024 by providing QA & GMP Consulting, Auditing & Training services as well as MasterControl solutions "Qx" electronic Quality Management Systems (eQMS) & "Mx" Manufacturing Execution Systems (MES) with electronic Batch Records (eBR).
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).
This article was originally published by SeerPharma's business partner MasterControl and is republished in-part here with their permission.
INFOGRAPHIC: A snapshot of how SeerPharma supported its customers with Quality and GMP Best-Practices in 2022.
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