Events

JAPM in collaboration with JFDA Announces the opening of Registration for the: “Herbal & Natural Pharmaceutical Products, Vitamins & Minerals Workshop” Join us for this exciting workshop to learn about: Updated regulations of Herbal Pharmaceutical Products & Vitamins Improve Registration Files according to the updated Registration Guidelines & Most Common Deficiencies & Observations based on JFDA Reports Who Should Attend: Regulatory Affairs Professionals R&D Professionals Quality Control & quality Assurance Professionals @ Pharmaceutical Companies & Regulatory Affairs Professionals @ Drugstores Speakers: JFDA/ Drug Directorate Pharmaceutical & Natural Products Unit
Join us for this exciting workshop to learn about: Updates on JFDA Accession to PIC/S The Impact of JFDA Accession to PIC/S on GMP Inspection Changes in Inspection of Quality Systems in relation to PIC/S How to Avoid Most Common Deficiencies in GMP Inspection JAPM with the support of JFDA & IFC Announces the opening of Registration for the: " JFDA Accession to PIC/S & Changes in Inspection of Quality Systems in Pharmaceutical Manufacturers Workshop” Who Should Attend: Quality Assurance Quality Control Technical Managers & Regulatory Affairs staff @ Pharmaceutical Companies Speakers: JFDA Inspection Team
JAPM with the support of IFC Announces the opening of Registration for a Virtual Workshop: “Continuous Improvement and the Quality System” The PIC/s GUIDE TO GOOD MANUFACTURING PRACTICE FOR MEDICINAL PRODUCTS PART I refers to ‘Continuous Improvement’ as an integral part of a Quality Management System. It states that “Product realization is achieved by designing, planning, implementing, maintaining and continuously improving a system that allows the consistent delivery of products with appropriate quality attributes”. This course is designed to provide an overview of the origin of the concept of continuous improvement as it relates to a Quality System and how
JAPM with the support of IFC Announces the opening of Registration for a Virtual Workshop: “Quality by Design Workshop” The course will cover: The principles of QbD and how they apply in the pharmaceutical manufacturing industry QbD terminology and process How QbD fits into the product development process The importance and impact of adopting QbD early in the product development phase How QbD is viewed from the regulators and how it aligns with regulator expectations Potential cost savings and business benefits from QbD implementation Implementation considerations (costs, training, leadership commitments and behaviour/culture modifications. This interactive workshop also provides participants the
JAPM in collaboration with JFDA, announces the opening of Registration in: All you need to know about: “Pricing of Pharmaceutical Products in Jordan” Speakers: JFDA Who should attend: Regulatory Affairs Professionals R&D Professionals, @ Pharmaceutical Companies For registration & more information email: dana@japm.com or call JAPM offices on +962 6 5413114
JAPM in collaboration with JFDA, announces the opening of Registration in: Hands-on Topical Medications workshop Speakers: JFDA Who should attend: Regulatory Affairs Professionals R&D Professionals, Quality Assurance, Quality Control Quality & Compliance @ Pharmaceutical Companies Date & Time: Monday: June 13th, 2022 9:00 am – 2:30 pm Venue: Crowne Plaza Hotel For registration & more information email: dana@japm.com or call JAPM offices on +962 6 5413114
JAPM with the support of IFC Announces the opening of Registration for a Virtual Workshop: “Fundamentals of Cleaning Validation Workshop” Purpose of this Course Upon completion of this course participants will have a basic understanding of: Current global regulations and requirements, including HBEL Cleaning process and method design, equipment design and qualification The limitations and use of visual inspection for cleaning validation Residue determination, analytical methods, and limit calculations Sampling, inspection, and testing for cleaning validation The documentation used to support an effective cleaning program. Common issues and how to deal with failures during the cleaning program. Who should attend
JAPM in collaboration with JFDA & USP, announces the opening of Registration in: “Biosimilars Workshop" Speakers: JFDA & USP Who should attend: Quality Managers and Authorised Person(s) Quality Control Managers Operations Managers RA Managers GMP Team Leaders R&D Team Leaders Department Heads @ Pharmaceutical Companies For registration & more information email: dana@japm.com or call JAPM offices on +962 6 5413114
JAPM with the support of IFC Announces the opening of Registration for Two Virtual Workshops: “Computer System Validation Workshop” & “Process Validation workshop” Registration is open for one or both Who should attend: Quality managers and personnel responsible for reviewing validation Quality personnel involved in the management of ongoing process verification programs Validation personnel at all levels Operational staff with responsibility for executing validation Employees who design, validate or administer GMP computerised systems End users of GMP computerised systems with involvement in the validation process Validation staff with limited or no computerised systems experience, looking to widen their knowledge @
biological
JAPM with the support of IFC Announces the opening of Registration for the Virtual Workshop: “Fundamentals of Biological Drugs Workshop” Who should attend: Quality Managers and Authorised Person(s) Quality Control Managers Operations Managers RA Managers GMP Team Leaders R&D Team Leaders Department Heads @ Pharmaceutical Companies “Fundamentals of Biological Drugs workshop” will help you to understand: Upon completion of this Fundamentals for Biological Drugs training course participants will understand. What is a Biologically Derived Drug and how does it differ from a synthetic drug? PIC/S clauses and Annexes that refer to such products Differences between WHO and PIC/s for biological