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
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