Events

PIC/S GMP Training Course PE 009-13

UpcomingGACP/GMP Training – Sydney

GACP (Good Agricultural and Collection Practices) and EU GMP (Good Manufacturing Practices) Introduction to regulations and compliance in the medicinal cannabis industry. Discussion of quality management systems (QMS), including hygiene, what makes a batch, batch traceability, basic record keeping (Good Documentation Practices or GDocP), quality risk management and Corrective and Preventive Actions (CAPA) Good Agricultural (more…)

  • GACP/GMP (SYD 24/04/20)
    24/04/2020
    9:00 am - 4:00 pm

5 Top Cannabis Cultivation Tips

UpcomingMedicinal Cannabis Cultivation Training – Auckland

Medicinal Cannabis Cultivation Training Course This Medicinal Cannabis Cultivation Training Course focuses on the cultivation, production and manufacture of Medicinal Cannabis, the practical questions around the most efficient facility design, your design choices within the design constraints of the regulators. In addition as you design, build, validate and operate your Medicinal Cannabis facility, you will (more…)

  • MCC (ACK 28/04/20)
    28/04/2020
    9:00 am - 4:00 pm

PIC/S GMP Training Course PE 009-13

UpcomingGACP/GMP Training – Auckland

GACP (Good Agricultural and Collection Practices) and EU GMP (Good Manufacturing Practices) Introduction to regulations and compliance in the medicinal cannabis industry. Discussion of quality management systems (QMS), including hygiene, what makes a batch, batch traceability, basic record keeping (Good Documentation Practices or GDocP), quality risk management and Corrective and Preventive Actions (CAPA) Good Agricultural (more…)

  • GACP/GMP (ACK 29/04/20)
    29/04/2020
    9:00 am - 4:00 pm

iso 13485

UpcomingQuality Management Systems – ISO13485 Training – Melbourne

Melbourne Quality Management Systems – ISO 13485 training course includes 2016 release This one day ISO 13485 training course covers the requirements of ISO 13485 and its implications within a medical device manufacturing company. PharmOut’s consultants regularly design and write Quality Management Systems for companies, from the smallest to the large blue-chip companies. They have (more…)

  • QMS - ISO 13485 (MEL-06-05-20)
    06/05/2020
    9:00 am - 4:00 pm

iso 13485

UpcomingQuality Management Systems – ISO13485 Training – Sydney

Sydney Quality Management Systems – ISO 13485 training course includes 2016 release This one day ISO 13485 training course covers the requirements of ISO 13485 and its implications within a medical device manufacturing company. PharmOut’s consultants regularly design and write Quality Management Systems for companies, from the smallest to the large blue-chip companies. They have (more…)

  • QMS - ISO 13485 (SYD-13-05-20)
    13/05/2020
    9:00 am - 4:00 pm

Process Validation Training

UpcomingProcess Validation Training – Sydney

Sydney Process Validation Training This one-day Process Validation training course is designed to provide an overview of the latest concepts and guidance documents for Process Validation as issued by the US FDA in 2011 and the EU and PIC/S Annex 15 in Qualification and Validation in October 2015. The aim of the course is to (more…)

  • Process Validation (SYD-20-05-20)
    20/05/2020
    9:00 am - 4:00 pm

Process Validation Training

UpcomingStatistics for Process Validation Training – Sydney

Sydney Statistics for Process Validation Training Statistics may not be for everyone but they are a fundamental part of GMP and all stages of process validation. We have developed an interactive course that will keep you engaged throughout the day as you develop a practical understanding through workshops and discussion of statistics in process validation (more…)

  • Stats for Process Validation (SYD-21-05-20)
    21/05/2020
    9:00 am - 4:00 pm

Quality Risk Management Training (ICH Q9)

UpcomingQuality Risk Management Training (ICH Q9) – Melbourne

Melbourne Quality Risk Management Training (ICH Q9) This Quality Risk Management (QRM) course is focused on how the QRM regulations apply to everyday pharmaceutical and biotech manufacturing processes and to accurately assess the risk to product quality and patient safety. As discussed at the International Council for Harmonisation of Technical Requirements for Registration of Pharmaceuticals (more…)

  • QRM ICHQ9 (MEL-02-06-20)
    02/06/2020
    9:00 am - 4:00 pm