Leadership

A dedicated and professional team which ensures the utmost high level of protocol management to the customer’s satisfaction.
IMP’s team works under strict GMP regulations to assure safe, high-quality and cost-effective product.

Amir Malka

Amir Malka

Chairman & Co-Founder

Amir has been working in the life science industry for over 20 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, Amir has been driving inPACK’s vision since the company’s inception in 2009, and will continue to do so for IMP. Amir 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.

Limor Teomim

Limor Teomim

CEO

Limor 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. Limor, 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, Limor held a position in QA of Starting Materials at RAFA Laboratories Ltd. Limor holds a MSc. Pharm in Pharmaceutical Chemistry and a BSc in Chemistry from The Hebrew University of Jerusalem in Israel.

Sofi Glam

Sofi Glam

Head of Project Management

Industry Experience
Sofi has more than 8 years’ experience in the pharmaceutical industry with over 6 years’ experience in the clinical supply management field. She serves as a clinical supplies subject matter expert and is a consultation focal point for various in-house interfaces and clients. As the Head of the Project Management Department, Sofi is responsible for the full IMP team of project managers.
Project Descriptions
Sofi is responsible for designing, planning, executing, and managing supply chains for worldwide clinical studies in all clinical phases in accordance with international guidelines and regulations, including GMP, GDP, and GCP guidelines. Sofi supervises the management of inventory, resupplies, and high-end cold-chain shipments for a number of top pharma companies. She is an expert in building effective customized project plans per customer needs while aligning both internal and external interfaces to ensure a timely delivery within the customer provided specifications, quality standards, and local and industry regulations. Plans include packaging, kit design, and labeling performed for both global and domestic studies. Sofi has Global supply management responsibilities and has vast experience in un-blinded supply management for both local and global studies as well as extensive experience managing work performed by contract manufacturing organizations (CMOs) and in integrating the needs of the CMO with the client needs to deliver clinical supplies in accordance with predefined deadlines.

Anna Schwartz Mor

Anna Schwartz Mor

Responsible Pharmacist

Anna has been in Pharmaceutical Services and Management for over 15 years. She has extensive knowledge and experience in Pharmaceutical regulation, Pharmaceutical Production, Patient-Centric drug preparations and Clinical Trials Management. As the former Deputy Director of Pharmaceutical Services at Tel Aviv Sourasky Medical Center (Ichilov), she led a team of professional Pharmacists and developed procedures to enhance Quality and Safety.

Anna holds a Master in Pharma and a Master of Business Administration (MBA). She is a Certified Quality Auditor (CQA) and a Certified Manager of Quality/Organization Excellence (CMQ/OE).

Bat-El Darmon

Bat-El Darmon

Quality Assurance Manager

Bat-El has over 12 years of experience in the pharmaceutical industry of commercial Medicinal Products of Israeli’s companies and Global company with logistic centers. Bat-El filled different QA positions and have experience with cGMP, GDP, ISO and local regulations.
Bat-El’s QA positions also included managing the QMS elements, SOPs writing, investigations, implementation of changes, Risk-Assessment, security information, audit and qulifications of suppliers.
As part of the QA position she gained experience with defined process as storage, distribution and re-labeling following the relevant regulations. Bat-El holds a B.A in Health Systems Management from Ariel University and attended several professional courses including internal and external auditing from the SII, GCP course from Bioforum and Risk-Assessment.

Lilach Levinson

Lilach Levinson

Warehouse Manager

Lilach has 30 years of logistics experience including many years in the pharmaceutical industry working under a strict GDP environment. Lilach has successfully passed numerous audits in the storage and distribution area. She has served as Dispatch/Warehouse manager at World Courier. Lilach has High analytical abilities, planning and finding solutions in real time as well as managing priorities within time constraints.
Lilach is responsible for the on-going Clinical Supply Management (CSM) of the Warehouse according to GMP, GDP principles and IMP SOPs. She also manages the Medical Cannabis inventory according to Israeli Medical Cannabis (IMC) unit requirements.

Dr. Maayan Cohen

Dr. Maayan Cohen

Dr. Maayan Cohen has over 15-years experience in marketing and business development in the biotech industry. She has held multiple managerial and business development positions in top industry companies and gained experience in streamlining a company’s vision into practical and concrete targets. Through her vast background working in laboratory environments, she is experienced with the strict accreditation and certification procedures necessary in all areas of the pharma industry (GLP, GMP and ISO 17025).
As a cannabis consultant, Maayan has been responsible for coordinating R&D, production, marketing, and sales and regulation for local as well as international clients. Her experience and knowledge enable Maayan to lead processes from initial vision through implementation. She makes a significant contribution to advancing procedures and making scientific knowledge accessible to management and the business sector.

Dr. Maayan Cohen holds a PhD in Chemistry and an MBA in Business Administration, specializing in marketing, from Bar Ilan University.