Research & Development

Surya Advanced Research & Development Centre, Banur

At Surya Pharmaceutical, we understand the value of continuous innovation in our products, services and methodologies. The company invests generously on its Research & Development facilities and has established state of the art laboratories at its production units to foster the development of products that would further enhance good health and well being.

The R&D centres at the company are approved by the Department of Science and Industrial Research, Government of India and are capable of extensive research for all products covered in the patents. The company recruits, trains, and motivates the highest calibre of scientists, lab technicians and personnel to ensure the development of new and improved formulations that would eventually the mass delivery of healthcare at reduced costs to the wider population. An integral facet of the R&D activities revolves around the reduction of stages and time to market of high quality products while maintaining the effectivness of its products at all times.

Products under development

  APIs   INTERMEDIATES
           
  arrow Cefdetoren Pvoxil   arrow Bicyclo Ketones(BCK)
  arrow Ceftibuten   arrow CDCA
  arrow Ceftizoxime Sodium   arrow 7-ATCA
  arrow Cefminox Sodium   arrow 7-ACT
  arrow Cefoxitim Sodium   arrow 7-TDA
  arrow Quinidine Sulphate   arrow Ceftezole free acid
  arrow Lysergol      
  arrow Nicergoline      
  arrow Cabergoline      
Formulation development
The latest addition in the CRAMS business is an ultramodern formulation development facility which shall be extending support to the expanding NDDS demand globally. The formulation facility shall be developing products encompassing the following parameters
  • Pre-formulation Studies
  • Formulation Development
  • Process Development
  • Packaging Development
  • Process Scale-up
  • Exhibit / Submission / Pivotal Batches
  • Comparator Product Modifications
  • Technology Transfer
  • Commercial Supplies Manufacturing
  • Co-ordination with CROs for BE Studies
  • Analytical Services
  • Regulatory Management
  • Intellectual Property Management
The formulation development facility shall be developing products in the following categories.
  Tablets
  arrow   Dispersible for Pediatric
  arrow   Orally Disintegrating
  arrow   Immediate Release
  arrow   Double layer
  arrow   Modified Release
  arrow   Targeted Release
  arrow   Film Coating
  Capsules (Hard Gelatin)
  arrow   Immediate release
  arrow   Modified Release
  Beads
  arrow   Beads Forming by Extrusion and Spheronaisation
  arrow   Drug layering by Tangential Coating
  arrow   Taste Masked Beads in a Stick Pack for Pediatric
  arrow   MUPS (Multi Unit Pellet System)
  Dry Syrups
  arrow   Taste Masked Dry Syrup for Pediatric
  Liquid Oral
  arrow   Clear Liquids/syrups
  arrow   Suspensions
  arrow   Emulsions
  Topical Applications
  arrow   Creams
  arrow   Gels
The cGMP facility is equipped with ultra modern equipment which can be scaled up easily in pilot and commercial scale easily.

Well trained and experienced manpower, clear cut developmental protocols supported by analytical development lab for method development, stability ably guided by a documentation and regulatory department compliments the efforts.

 

Research & Development
 
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