SeerPharma at ISPE South Asia Pharmaceutical Manufacturing Conference

August 19, 2019
by SeerPharma

SeerPharma is excited to announce that we will be attending and exhibiting at the 2019 ISPE South Asia Pharmaceutical Manufacturing Conference, in Bangalore, India. The event is running from 25th to 27th September 2019.


The conference will focus on the product lifecycle approach to Quality, from drug development to post-market approvals. Topics will include critical approaches for successful manufacturing and leveraging quality as a competitive advantage. Speakers will include pharmaceutical and biopharmaceutical industry professionals along with regulators from FDA, MHRA, and APAC regions who are subject matter experts in quality and compliance.

Come and meet us in Bangalore to learn about:
  • MasterControl – Electronic Quality Management System (eQMS) platform used by the US FDA
    • Document Control
    • Training Management
    • Change Control
    • Corrective and Preventive Action (CAPA)
    • Audit Management
    • ...and more
  • Online Postgraduate Qualifications in GMP from the University of Technology Sydney
    • Certificate in GMP
    • Diploma in GMP
    • Masters in GMP
  • Expert training and advice for your staff on how to prepare for and respond to regulatory GMP inspections
Who Should Attend the Conference:
  • Regulatory Affairs experts
  • GMP Inspectors
  • CMC professionals
  • Manufacturing and Operations professionals
  • Quality Assurance professionals
  • Quality Control professionals
  • Pharma Senior Level Managers
  • Executive Level Leaders in Pharmaceutical and Bio Manufacturing
Conference Learning Objectives
  • Become current on industry trends in quality & quality risk management
  • Understand quality and regulatory requirements and expectations
  • Address the recent developments and innovations in manufacturing
  • Understand the necessary elements for on-going quality sustainability
Some Agenda Items
  • Trends in Quality and Compliance
  • Quality and Compliance: Addressing Risk Mitigation
  • Trends in Cleaning Validation, Process Validation and Controls
  • Out-of-Specification (OOS) Investigations
  • Developments in Aseptic Processing
  • Data Integrity Across the Lifecycle
  • Understanding Quality: Where does GMP Begin?
  • Remediation: Moving from Uncertainty to Robust Sustainability in CGMPs

We look forward to meeting you in Bangalore, in September.

For more information on the event, please visit: 

Filed Under: ISPE, Conference