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Nextar CDMO- drug and medical devices development and manufacturing services, GMP and ISO13485 certified

Your innovative product

our creative solutions


Your product development journey requires both experience and expertise. In order to help you on this journey, we offer you a customized development package, based on your needs and the regulatory phase. As a well-experienced drugs and medical devices Contract Development and Manufacturing Organization (CDMO), we will help you get to the clinic in the most rapid, high quality, and cost-effective way.


When going on a clinical trial, your product needs to meet the regulatory requirements. We were successfully audited by the FDA so you can be assured that our full range of services is in compliance with the regulatory requirements (GMP, ISO13485, and IMC-GMP).


Born out of Nextar, Nextage Therapeutics Ltd. is a global pharmaceutical company bringing the scientific clarity and confidence needed to develop the next generation of cannabinoid-based products.


Nextage addresses existing markets with products that stand out and provide clear unique added value with real immediate commercial potential

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Manufacturing Services

About Us

Nextar Chempharma Solutions Ltd. is a company specializing in drugs and medical devices development and manufacturing. We use our vast knowledge to advance our clients by providing fully integrated drugs and medical devices Contract Development and Manufacturing services (CDMO). As a service provider, we are guided by two major principles: quality of work and cost-effectiveness.

By combining chemical synthesis, formulation development, and analytical testing with GMP manufacturing and packing for clinical trials, we offer our clients a one-stop-shop for all their development needs.

Read more about what you gain by working with us.

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13B Einstein St.

Weizmann Science Park

Ness Ziona


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