Contract Development Services
SciVac Ltd. has the facilities and expertise that enable development of therapeutic proteins starting with a selected clone, through production, purification, and analytical testing. For your phase I and II clinical trials, SciVac Ltd. offers manufacturing services under cGMP conditions.
Development Services
- Production processes in bacteria
- Production processes in mammalian cells
- Purification processes
- Filling processes
- Analytical services
Manufacturing Services Under cGMP conditions
- Production Processes in bacteria or mammalian cells
- Purification processes
- Formulation and Filling processes
- QC release testing
- Manufacturing is suitable for Phase I & Phase II clinical trials
Analytical Development Capabilities
Highly advanced technologies for testing raw materials, in-process controls and release testing in full compliance with EP/USP pharmacopeia and ICH guidelines, such as:
- HPLC
- Immunological Assays
- Colorimetric Electrophoreses
- SDS-PAGE, Western Blot
- Activity/Potency assays
- Bioassays
- Microbiology
- Others, tailored to the client’s needs
SciVac Ltd. Offers
- Experienced scientists and manufacturing professionals
- Effective, robust and timely development
- Modern facilities and state of the art clean rooms
- Proven record for on-time delivery
- Competitive pricing
Contact Us
SciVac Service Unit
Gad Feinstein Rd.
P.O. Box 580
Rehovot, Israel 7610303
info@scivac.us
+972-8-948-0625/614/664
