We provide the global community with small molecule, biologics, organic treatments and medicines. Through innovative state-of-the-art personalized medicines, we seek to cure and prevent common and rare diseases for diverse individuals in rural and urban communities. SanKav is a CMO, CDMO, Contract Laboratory Services provider for Testing of In-vitro and In-vivo samples that includes CRO services of bioavailability, pharmacokinetic, bio-equivalence and clinical programs testing. Our services include R&D, manufacturing, validation and testing of API/ drug substances, intermediates and finished dosage forms of small molecules and biologics, and associated materials such as excipients, bioprocessing aid materials and packaging components. SanKav provides services for FDA and other regulatory submissions and FDA correspondences. Our biologics technology platforms include the following: Antibody therapies and processes [mAb, bi-specific mAb, and mAb fragments] Vaccine delivery [DNA vaccine, viral vector vaccines, inactivated viral vaccines, recombinant protein vaccines, virus-like particles (VLP), nanoparticle vaccines and mRNA vaccines] Supporting processes [plasmid and viral vectors such as adeno, adeno-associated, and lentiviral] Cell and gene therapies [autoimmune, cardiovascular, neurological, adeno-associated virus (AAV) based therapy, CAR-T cell therapy, CRISPR] Adapt to new product modalities [flexible workflows for mAb, AV, pDNA, and mRNA] Aseptic fill finish-vial, PFS Our additional complex laboratory testing/ test certificates (CoA) include: Comprehensive laboratory testing for Plant-Based Products, package containers, bags, etc. including Pesticides Full testing for the Petroleum and Hydrocarbon based materials, products, package containers and bags, tubing, etc. Extractables & Leachables Tests to support the Environmental Protection Agency (EPA) samples including water testing (well water, city water) for companies, town, county and state.