7M4C6519QA Auditor

Osnat has 5 years of experience in the quality assurance department in accordance with SOP's and work instructions as documentation processes administrator, in at Teva Pharmaceutical Industries. She has extensive experience working under strict GMP environment and an overall responsibility of cross-company documentation processes of drug manufacturing and handling.
Osnat holds a B.Sc. in Life Sciences, Bar-Ilan University and an MBA in Bio-Medical Management program, at The College of Management at Rishon Lezyon.

OrlyMordechayPlanning & Control Manager

Mrs. Mordechay has 12 years of experience in the pharmaceutical industry in the quality department working under strict GMP environment. Mrs. Mordechay has served as a documentation & training coordinator for LycoRed Bio and Nesher Solutions, companies specializing in development and production of sustained released micro-encapsulated, solid dosage forms. Mrs. Mordechay has 5 years of experience as a  packaging team leader at inPACK and in her current position at IMP establish & issue IMP work plan and ensure its execution.  

YaacovNimrodiWarehouse Manager

Mr. Nimrodi has over 30 years of experience in the pharmaceutical industry working under strict GMP environment. Mr. Nimrodi has successfully passes numerous audits of regulatory agencies, both European, American and Israelis in the storage and distribution area. Mr. Nimrodi has served 23 as warehouse senior employee & manager at InterPharm Company and 5 years as Colbar LifeScience (JnJ group) warehouse manager


AmihayZolkovSenior Project Manager, QP and Responsible Pharmacist

Mr. Zolkov has over 7 years of experience in the clinical supplies management field working at big pharma industry. During these years he has managed the supply chain of several clinical studies in various phases, including multi-national studies. Mr. Zolkov has experience in writing clinical supply chapters in the study protocols, design of study kits and coordinating activities related to clinical supplies management including label design, IRT specifications, packaging planning, and distribution setup. Mr. Zolkov holds an M. Sc in Physiology and Pharmacology from Tel Aviv University and a B. Pharm from the School of Pharmacy in The Hebrew University in Jerusalem. Mr. Zolkov is a QP

LimorTeomimQA Director

Mrs. Teomim has over 20 years of experience in both manufacture and development of commercial and Investigational Medicinal Products within the pharmaceutical industry, quality management system, cGMP, GDP and local regulations. Mrs. Teomim, certified by both the American and Israeli quality societies as a Certified Manager of Quality (CMQ), has served as a Quality Manager for LycoRed Bio and Nesher Solutions, companies specializing in development and production of sustained released micro-encapsulated, solid dosage forms. Prior to that, Mrs. Teomim held a position in QA of Starting Materials at RAFA Laboratories Ltd. Mrs. Teomim holds a MSc. Pharm in Pharmaceutical Chemistry and a BSc in Chemistry from The Hebrew University of Jerusalem in Israel.

RonnieRosenBD Director, QP

Mrs. Rosen has been working in the pharmaceutical industry for 20 years, with 12 years of experience in both clinical & commercial supply chain fields, from portfolio picking stage till product launch in new markets. Mrs. Rosen has managed global clinical trial supply chains of different study phases and scales, blinded and open-label designs with various packaging configurations all under strict cGMP and GDP principles. Today, Mrs. Rosen brings her extensive experience in clinical supply to the set up & contract phase with new customers and their specific needs. Ms. Rosen holds an M.A. in Health Administration from Ben-Gurion University, and B.Sc. in Pharmacology from Hebrew University of Jerusalem. Mrs. Rosen is a QP.


Mr. Malka has been working in the life science industry for over 18 years and is the founder of Bioforum Ltd.. In 2015, together with SLE he established IMP, which originated from the supply management operation of Bioforun, previously known as inPACK- a GMP certified facility for clinical supply management services. With his deep expertise in clinical trials and understanding of supply challenges, Mr. Malka has been driving inPACK's vision since the company’s inception in 2009, and will continue to do so for IMP. Mr. Malka holds a L. LB and is a member of the Israeli Bar Association. He is also a member in a number of life science and clinical trials associations, thriving for the removal of barriers and the promotion of these industries in Israel.