InvaTech Pharmaceuticals
Research-driven specialty pharmaceutical company focused on developing, manufacturing and marketing generic prescription products. Operates a cGMP-capable facility configured for ANDA-scale manufacturing and provides formulation development, regulatory dossier support, packaging for solid and liquid dosage forms, and contract manufacturing via international manufacturing partners.
Industries
Nr. of Employees
small (1-50)
InvaTech Pharmaceuticals
40 C Cotters Lane, Suite # A, East Brunswick, NJ 08816
Products
Generic Prescription Products
Generic prescription medications developed, manufactured, and marketed by InvaTech Pharmaceuticals for various therapeutic uses.
Pharmaceutical Manufacturing Services
Manufacturing services for generic pharmaceuticals including tablets, capsules, and liquid formulations under cGMP standards.
Regulatory Affairs Support
Support services for regulatory compliance and filing related to generic pharmaceutical products.
Generic Formulation Development
Development services for generic drug formulations to replicate branded medications.
Generic Prescription Products
Generic prescription medications developed, manufactured, and marketed by InvaTech Pharmaceuticals for various therapeutic uses.
Pharmaceutical Manufacturing Services
Manufacturing services for generic pharmaceuticals including tablets, capsules, and liquid formulations under cGMP standards.
Regulatory Affairs Support
Support services for regulatory compliance and filing related to generic pharmaceutical products.
Generic Formulation Development
Development services for generic drug formulations to replicate branded medications.
Services
Development services for generic formulations to prepare products for manufacturing and regulatory filings.
cGMP-capable manufacturing for ANDA-scale production, including tablets, capsules and liquid fills.
Compilation of regulatory dossiers (DMF, ANDA, 510(k)) and advisory services on current FDA expectations.
Packaging capabilities for tablets, capsules and liquid products into commercial containers.
Coordination with exclusive manufacturing partners to provide cost-competitive production and commercial scale services.
Development services for generic formulations to prepare products for manufacturing and regulatory filings.
cGMP-capable manufacturing for ANDA-scale production, including tablets, capsules and liquid fills.
Compilation of regulatory dossiers (DMF, ANDA, 510(k)) and advisory services on current FDA expectations.
Packaging capabilities for tablets, capsules and liquid products into commercial containers.
Coordination with exclusive manufacturing partners to provide cost-competitive production and commercial scale services.
Expertise Areas
- Generic drug development
- Formulation development
- cGMP manufacturing and scale-up
- Regulatory compliance and dossier preparation (DMF, ANDA, 510(k))
Key Technologies
- cGMP manufacturing
- Generic formulation development
- ANDA/DMF/510(k) regulatory submissions
- Solid dose and liquid dosage packaging