ANWITA R & D CENTER

A state of Art facility with fully equipped for development of various dosage forms and NDDS formulations. Located on a spacious 20,000 SFT research and development Center is the hub of focused scientific activity, wherein the operational teams develop, optimize technological solutions and also ensure these innovations are scalable.

Pharmaceutical Development strengths:

Aqueous Granulation

Dry Granulation

Spray drying

Direct compression

Bi-layered tablet compression

Tablets compression from  70 mg  to 1500mg  weight

Fluid bed processer  ( Top spray  and Bottom spray)

Microencapsulation technology

All types of coating technology

Micro pellets and normal pellets development technology

Hygroscopic and low bulk density active handling capabilities

Table top liquid filling machine

Small scale Ointment unit

Separate set-up for development  of  Oncology / depot-Injections

Separate set-up for development of contraceptive Injectable

Analytical development facility

Anwita having state of art analytical instruments and equipments to handle complete analysis of above said dosage forms.

MANUFACTURING FACILITIES

Anwita manufacturing facility consisting of 3 modules to cater PFIs, Tablets , Capsules

CHEMISTRY CAPABILITIES:

  • Alkylation
  • Asymmetric Synthesis
  • Bromination (Allylic and Dehydro Bromination)
  • Catalytic Hydrogenation
  • Chloro Methylation
  • Cyanations
  • Diazolization
  • Friedel Crafts Reaction
  • Halogenation-PCl3,PCl5,POCl3,SOCl2
  • Heterocycles Build-Up
  • High Temperature and Low Temperature reactions
  • High Pressure Reaction
  • Indole Chemistry
  • Nitrations & Nitrasonations
  • Oxidation-Metallic and Catalysed
  • Reduction
  • Variety of Organic Reactions
  • Transesterification
  • Grignard Reactions
  • High Vacuum Distillation
  • Knoevenagel condensation 

REGULATORY CAPABILITIES: 

  • Proficiency in developing Analytical Methods ( HPLC & GC )
  • Capability to Validate Analytical Methods
  • Synthesize and Characterize Impurities and Working Standards
  • Understanding of IPR & Regulatory Criteria for example Developing non infringing route of Synthesis,Different Polymorphism etc.
  • In-house Interpretation of NMRs,LCMs.etc.
  • Dossier Development & Technology Transfer
  • Pre-formulations studies
  • Non-infringing patent formulations
  • Process development and validations
  • Stability studies
  • Analytical method development and validations
  • Dissolutions and impurity characterization
  • Packing compatibity studies
  • A complete dossier development along with technology transfer at site