Vitae Enim Vitae Scientific
VeV Scientific, Inc. is a California-based life science company dedicated to supplying necessary tools and components to scientists, manufacturers, and customers in a timely, efficient manner. The company specializes in contract manufacturing for pharmaceutical products, including drug manufacturing, lyophilization, sterile injectables, and tablets and capsules. With a diverse team experienced in various industry sectors, VeV Scientific aims to intersect technology with regulations to set standards in compliance and quality.
Industries
Nr. of Employees
small (1-50)
Vitae Enim Vitae Scientific
Products
cGMP Sterile Injectables
Formulation and aseptic fill/finish services for sterile injectable commercial products and clinical trial materials, including liquid filled vials, lyophilized vials, pre-filled syringes or cartridges, and large or small volume parenterals.
USP Sterile Purified Water
Sterile purified water intended for use in various biologics, drug, and medical device manufacturing applications.
Drug Security Chain Supply Act (DSCSA) packaging solutions
Packaging services providing standardized, unit-level traceability of pharmaceutical products along the entire drug supply chain to comply with the Drug Security Chain Supply Act (DSCSA).
Pharma Drug Manufacturing
Contract Prescription and OTC pharmaceutical manufacturing services registered with the FDA and inspected by the DEA and California Department of Public Health.
cGMP Custom Media Manufacturing
Custom media and buffer manufacturing service built to client formulas in a cGMP environment with batch sizes ranging from 500 mL to 100 liters.
Small-Vial Lyophilization Services
Small-vial lyophilization (freeze-drying) services in a controlled cGMP cleanroom providing consistent, repeatable results for research and manufacturing programs.
cGMP Sterile Injectables
Formulation and aseptic fill/finish services for sterile injectable commercial products and clinical trial materials, including liquid filled vials, lyophilized vials, pre-filled syringes or cartridges, and large or small volume parenterals.
USP Sterile Purified Water
Sterile purified water intended for use in various biologics, drug, and medical device manufacturing applications.
Drug Security Chain Supply Act (DSCSA) packaging solutions
Packaging services providing standardized, unit-level traceability of pharmaceutical products along the entire drug supply chain to comply with the Drug Security Chain Supply Act (DSCSA).
Pharma Drug Manufacturing
Contract Prescription and OTC pharmaceutical manufacturing services registered with the FDA and inspected by the DEA and California Department of Public Health.
cGMP Custom Media Manufacturing
Custom media and buffer manufacturing service built to client formulas in a cGMP environment with batch sizes ranging from 500 mL to 100 liters.
Small-Vial Lyophilization Services
Small-vial lyophilization (freeze-drying) services in a controlled cGMP cleanroom providing consistent, repeatable results for research and manufacturing programs.
Services
cGMP manufacturing of prescription and OTC liquids, semisolids (gels, creams, ointments), suppositories and controlled-substance products at small and large scale.
Small-vial freeze-drying with formulation support, cycle development, filling/labeling/packaging, in-process and final release testing, stability testing and microbial testing in a controlled cleanroom.
Aseptic fill/finish services for commercial and clinical sterile parenteral products, planned validated cGMP suite for multiple vial and syringe formats and serialized packaging prior to distribution.
Third-party quality arm services including cGMP assessments, GAP analyses, FDA 483 responses, compliance remediation, site transfer protocols, quality systems audits, regulatory submissions, and training.
Planned expansion into cGMP oral solid dose manufacturing supporting wet granulation, fluid bed drying, immediate- and extended-release tablets, coating and liquid gel caps with streamlined production to reduce waste.
Packaging services that include serialization and supply-chain traceability to support Drug Supply Chain Security Act compliance.
cGMP manufacturing of prescription and OTC liquids, semisolids (gels, creams, ointments), suppositories and controlled-substance products at small and large scale.
Small-vial freeze-drying with formulation support, cycle development, filling/labeling/packaging, in-process and final release testing, stability testing and microbial testing in a controlled cleanroom.
Aseptic fill/finish services for commercial and clinical sterile parenteral products, planned validated cGMP suite for multiple vial and syringe formats and serialized packaging prior to distribution.
Third-party quality arm services including cGMP assessments, GAP analyses, FDA 483 responses, compliance remediation, site transfer protocols, quality systems audits, regulatory submissions, and training.
Planned expansion into cGMP oral solid dose manufacturing supporting wet granulation, fluid bed drying, immediate- and extended-release tablets, coating and liquid gel caps with streamlined production to reduce waste.
Packaging services that include serialization and supply-chain traceability to support Drug Supply Chain Security Act compliance.
Expertise Areas
- Contract pharmaceutical manufacturing
- Lyophilization and freeze-drying cycle development
- Aseptic fill/finish and sterile injectables
- Oral solid dose (tablet and capsule) manufacturing
Key Technologies
- Lyophilization (freeze-drying)
- Aseptic filling / sterile fill-finish
- Wet granulation
- Fluid bed drying