• Developing Pharmaceutical Research Proposals

• Drug product development

• Market research

• Third party manufacturing guidance

• Developing Pharmaceutical Research Proposals

• Third party manufacturing and Troubleshooting consultation

We conduct GMP Compliance Audits of the manufacturing sites, GLP Audits (important to make certain suitability & capability of testing laboratories for its Quality Control, Infrastructure, Practices and the implementation of Data Integrity guiding principle).

Customized online guidance and training on various topics such as

Quality Management System (QMS), Audit, GMP, GLP,GDP, Data integrity (DI), Audit trail, deviations, CAPA, QbD, OOS, OOT, Change control, Analytical method transfers, Medical/Scientific writing, Pharma-Compliance, Elemental impurities, Nitrosamine impurities, Computerized System Validation (CSV), Intellectual Property Rights (IPR), Clinical trials, Drug Regulatory Affairs (DRA), Industry-Institute Interaction, 483’s, Risk assessment tools, Quality Risk Management, 5 Why’s?, 8D’s, Email writing and meeting etiquettes, etc.

Scientific communications- Pharmaceutical/other Healthcare field/s

• Research Project/proposal writing (as per the guidelines of various research granting agencies)/Post graduates (Pharmacy/Healthcare)/Ph.D. (Pharmacy/Healthcare) Synopsis/Thesis writing support

• Plagiarism checking and related support

• Medical Writing/content editing/proofreading

• Review article/Journal article/White paper

• Scientific report/Monograph

• Support with publication planning and/ journal submission

• Conference posters and conference proceedings

• Presentation Slide kits

• Educational material for Pharmaceutical/Healthcare professionals

• Letter of Recommendation (LOR) preparation support

• Prior art search, Patentability aspects

• Patent drafting and filing Provisional/Complete Specification

• Responses to examination Reports

• Patent Prosecution (Pre-grant, Post grant)

• Filing of (Patent Cooperation Treaty) PCT 7 Conventional application and execution

• Dossier Services

• Drug Master File (DMF) Preparation, Registration, Filing

• Clinical/Nonclinical/Technical Support, and related services

• Pharmaceutical Regulatory Affairs Trainings

• New Pharmaceutical business start-up guidance such a legal requirements, Company registration procedure, resource management, and relevant services

• Literature search and find up-to-date research

• Prepare evidence-based solutions

• Research report- Compilation and Preparation

• We have quick guide on how to do it

• Things to Know Before Starting

• What are the requirements for getting license ?

• Documents & Costings

• Interview Preparation services including related training

• Curriculum Vitae (CV)/Resume crafting, and

• Placement assistance/guidance services (For professionals of Pharmaceuticals field)