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Training for people who write or review documents; covering technical writing principles, trends & tools for writing effective SOPs & forms | Apr 2025 hubs.li/Q039Dvzh0

Learn techniques for preparing audit plans, performing audits, verifying observations, reporting and Corrective and Preventive Action (CAPA). hubs.li/Q03csZ2W0

We are proud to sponsor and chair BioMelbourne Network’s inaugural 2025 BioSymposium: Innovations in technologies – Implantables, Neurotech and Diagnostics hubs.li/Q03d0RzF0

SeerPharma is honoured to be a guest speaker on Contamination Control at Let’s Rethink the Future of Quality Control: A Charles River QC Micro Seminar hubs.li/Q03d1cR_0

Our strategic partner MasterControl helps you with a publication addressing 5 key checklists for AI Readiness for Life Sciences Organizations. hubs.li/Q03fsSw10

GMP Training: Learn effective failure investigations, root cause analysis & corrective and preventive actions (CAPA) to minimise quality issues. hubs.li/Q03gjmX10

Gain insights into key clauses & concepts that underpin a QMS being effective & compliant with the ISO 13485:2016 Standard: medical device QMS requirements hubs.li/Q03g3Stj0

Join us 24-APR-2025 for this informative webinar where we'll help you evaluate QMS options and determine the best solution for your organisation's needs. hubs.li/Q03jcJdL0

Learn current regulatory requirements with a 6-step plan to manage your supplier quality and ultimately reduce your risks & improve your compliance. hubs.li/Q03jrC5B0

Learn the current 'cleaning validation landscape' & gain insights applying a risk-based approach for compliant cleaning validation. hubs.li/Q03k06gs0

Conducting computerised system audit trail reviews before each batch is released is a risk-based approach to maintain compliance & operational efficiency. hubs.li/Q03kmQWl0

15-MAY-2025 | Learn how your team can harness AI to reduce time-to-market, avoid remedial actions and produce higher-quality products with fewer resources. hubs.li/Q03k-Sjp0

Learn PIC/S GMP Guide Annex 16 Authorised persons & batch release: Batch Review & Disposition, GMP Agreements, Audits, Process Control, Stability and more. hubs.li/Q03k_0150

Join us to gain some insights into the PIC/S GMP Guide Annex 1 Contamination Control Strategy (CCS) requirements to help you get your documentation ready. hubs.li/Q03lyj100

Exploring how Industry 4.0 principles can enhance data contextualisation, compliance-driven decision making & operational agility in regulated environments hubs.ly/Q03lZjst0

Learn the regulations and key elements of a system you need to effectively manage customer complaints, adverse events / reactions and product recall. hubs.li/Q03lZTZF0

Exploring the challenges and opportunities presented by rapid technological innovation in the Pharmaceutical and MedTech sectors. hubs.li/Q03n47nB0

Learn to apply best-practice Good Manufacturing Practices by stepping through key chapters of the PIC/S GMP Guide using case studies & industry scenarios. hubs.li/Q03n46Zb0

Mainstream support for SAP ECC6 ends in 2027 so Pharmaceutical and Medical Device manufacturers face a critical decision about upgrading to SAP S/4HANA. hubs.li/Q03p2KxD0

Learn the tools you need to navigate the various validation pathways you can take to make sure you get your Validation 'right first time'. hubs.li/Q03p8rfh0