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Our company provides superlative services to move your company’s life sciences projects forward from conception to validation, through development, pass regulatory hurdles, and into the marketplace.

1. Superlative BioSciences Corporation is a Biological Services Company that provides laboratory services in the area of in vitro toxicology. The company performs cell culture screening systems as a service-for-a-fee to companies within the pharmaceuticals, consumer goods, agricultural and cleaning products, chemicals, and medical device industries.
2. Superlative BioSciences Corporation also provides consultation on: Compliance to FDA, EU, and ICH GLP, GMP, QSR, GTP, GCP; Eligibility for FDA Regenerative Medicine Advanced Therapy (RMAT) Designation; CE Marking Services; and ISO Documents Management. This includes the Preparation of Quality Manuals & Other Quality Documents including Change Control, Deviations, Trending, CAPA, Root Cause Analysis, Complaint Handling, and Risk Management Plans. We also write SOPS, Master Batch Records (MBRs), Validation Plans & Reports.
3. We also prepare IRBs, Clinical Protocols, CMCs, INDs, BLAs, NDAs, 510Ks, PMAs documents and handle your company’s FDA regulatory submissions.
4. In addition, Superlative BioSciences Corporation provides the following Life Sciences Business Services: Writing & Editing of Proposals including SBIR & STTR Grants; Conducting Market Research and Preparing Marketing Plans, Business Plans, Pitch Decks and Written & Recorded Presentations to Get Your Projects Funded; Writing and Editing of Reports, Books, Articles and Online Study Guides.