JAPM with the support of JFDA & IFC Announces the opening of Registration for the Virtual Workshop: Data Integrity Workshop Data Integrity Training Course Data integrity is not new. It is implicit, and always has been, as a foundation of good manufacturing practice (GMP). The subject of data integrity, however, has an increased profile because hybrid (paper and electronic), digital technologies and electronic systems have become prevalent in modern manufacturing. Globally regulators are recruiting and training their Regulatory Compliance Inspectors in data integrity. During GMP compliance audits, Inspectors are identifying increasing numbers of GMP violations linked to data integrity. The
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To discuss in detail the implementation of the newly issued JFDA Annual Report Guidelines JAPM in cooperation with JFDA Announces the opening of the Registration in the: “Annual Report Workshop” Provided by JFDA Drug Registration Team Who should attend: Quality Assurance, Quality Control Technical Managers Quality & Compliance Regulatory Affairs Staff @ Pharmaceutical Companies For registration & more information email: dana@japm.com or call JAPM offices on +962 6 5413114 Attention: in order to attend the workshop, you should fit in one of the below categories as we strictly apply the government rules in this regard: Be fully vaccinated against COVID-19
In-Person workshops are back ! JAPM announces the opening of Registration in: Validation Requirements & Evaluation Workshop Provided by JFDA Validation Committee and JFDA QC Lab Team Targeted Audience: R&D personnel at pharmaceutical manufacturers “The workshop will be repeated in two dates. To comply with the National Defense Law in Jordan; we will accept the registration of a limited number of participants according to the capacity limit of the venue; kindly register in the one of the below dates” Monday: June 28th , 2021 or Monday: July 5th, 2021 Venue: Rotana Hotel- Amman For registration & more information email: dana@japm.com
JFDA, IFC, JAPM Announce the opening of registration for the: "PIC/S Inspection Procedures & Inspection techniques from the Industry's point of view” Workshop Who should attend: Quality Assurance, Quality Control, Technical Managers, Quality & Compliance Regulatory Affairs staff @ Pharmaceutical Companies For registration & more information please email: dana@japm.com
JAPM with the support of JFDA & IFC Announces the opening of Registration for the Virtual Workshop: “Remote Auditing Workshop” Who should attend: Quality Assurance, Quality Control Technical Managers Quality & Compliance Regulatory Affairs Staff @ Pharmaceutical Companies Questions this “Remote Auditing Techniques Workshop” helps answer: What do Auditee needs to know to prepare & get ready for a remote audit? What do Internal Auditors need to know in order to conduct a Remote Audit on their suppliers successfully? What are the benefits of conducting remote audits vs onsite inspections during a global pandemic, when onsite auditing is risky to
"PIC/S Inspection Procedures & Inspection techniques from the Industry's point of view” Workshop Who should attend: Quality Assurance, Quality Control, Technical Managers, Quality & Compliance Regulatory Affairs staff @ Pharmaceutical Companies Date & Time: March 31st, 2021- 09:00 am Fees: 200 JD members 250 JD nonmembers Group Discount: 10% for 3 or more 15% for 5 or more Venue: Zoom For registration & more information please email: dana@japm.com
Ensuring Quality and Integrity of APIs throughout product lifecycle workshop. book your calendar and register in: " API Requirements/ Recent Developments Workshop” Topics: JFDA Requirements for API Manufacturers approval (New Submission) JFDA Requirements for Addition of Alternative API Manufacturer (Post Approval Changes) Nitrosamine Impurity in some APIs Who Should Attend: API sourcing professionals Regulatory affairs experts R&D experts Manufacturing and operations professionals Quality assurance professionals Quality control professionals CMC professionals Date: To be determined Venue: JAPM Training Room Fees: JAPM Members: 200 JD Non JAPM members: 250 JD For registration & more information email: dana@japm.com or call JAPM offices on
JAPM in collaboration with JFDA Announces the opening of registration for the workshop: “Pharmacovigilance In Practice” Speakers: JFDA/ Pharmacovigilance Dept. Who Should Attend: QP for Pharmacovigilance & Regulatory Affairs staff at pharmaceutical companies Fees: JAPM Members: 150 JD Non JAPM members: 200 JD