Consultancy & Services

HEALTHCARE MANAGEMENT AND ADMINISTRATION

The healthcare industry is growing at a rapid pace with healthcare becoming a pivotal issue and a point of focus. The industry is witnessing a lot of restructuring within existing setups, mergers and acquisitions taking place, rise of medical tourism and entry of new players to compete within this dynamic space. The challenge is to optimise the scarce and expensive resources, invest on high cost appliances and technology with a focus on uncompromised quality and treatment outcomes. Our effort is to help win this challenge by helping to use all the resources optimally to get the desired outcome.

Service Offerings:
  • Strategic planning and management
  • Health policy and economics
  • Healthcare quality and patient safety
  • Pricing models and strategies
  • Business restructuring and re-alignment
  • Product portfolio analysis
  • Branding and marketing initiatives
  • Business operations
  • Customer relationship management (customized patient relationship activities for hospitals, individual clinics and other setups)
  • Content writing for disease-specific patient educational materials and other patient awareness collaterals

 


Pharmaceuticals

The cutthroat competition within the pharmaceutical industry, changing regulations and guidelines, challenges faced for new drug development, and the need for creative marketing and tactical plans, to name a few, give rise to the need for each company to identify a niche to sustain and grow.

Getting the optimal product portfolio mix is therefore crucial.

Service Offerings:
  • Product Management
  • New product launch and re-launch
  • Product Portfolio Analysis
  • Marketing initiatives
  • Content writing for promotional collaterals, product manuals, etc.
  • Regulatory Affairs – Preparation of dossiers (CTD, DMF) for registration, marketing authorization and filing of pharmaceuticals – new drug molecules, generics, biosimilars, vaccines and biologics with FDA. Liaising with DCGI office, Zonal CDSCO, State FDA
  • Pre-clinical and Clinical Research Operations and Documentation, including preparation of dossiers for clinical trial applications for new drug molecules, generics, biologics, biosimilars, vaccines, etc.
  • Intellectual Property Management including drafting patent applications, freedom to operate analysis
  • Technical documentation for government funding applications
  • Vendor Certification Audits and GMP Audits
  • Establishment of a Quality Management System (QMS)
  • Scientific Writing and Documentation