What is the role of the Department of Pharmacy in the Ministry of Health?

2020-08-04T12:42:17+00:00December 27th, 2018|

The Department of Pharmacy at the Ministry of Health is the body responsible for prescribing drugs, importing drugs, pharmacist control, providing pharmacological information, approval and supervision of human clinical trials, research on the effects of drugs on humans, herbal medicine approval, homeopathic products and cosmetics. Medicines used in Israel must be registered in the Medicines Register. A drug will only be prescribed after its safety, efficacy and quality have been demonstrated.

Product Development, Delivery System & Clinical Trials

Novel cannabis products and delivery system for improved bio-availability, accuracy, consistency and efficacy that can be proven and backed up with a strong IP and clinical trials

Growing, Manufacturing & Lab Facilities Design

Conceptual & detailed design including personnel/material flow diagram, pressure cascade, cleanness level, utilities and technology based on current GxP standards and common practices

Quality Assurance & Good Practices (GxP)

An effective quality management system establishment, policies and SOPs writing, cultivation and manufacturing procedures, protocols and employees training

Cultivation & Product Manufacturing Technology

Utilities, systems, machinery and controls required for cultivation, development and manufacturing processes that will enable high quality, control and cost-effectiveness.

New Product Regulations & Submissions

Cannabis products specifications and regulatory requirements completion including all relevant documentation and data in order to be submitted and sold in regulatory markets

Qualification &Validation

New facility, infrastructure, utilities, system, machinery, software, control system, manufacturing/cleaning processes qualification and validation protocols, execution and reports

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