Book a discussion
Medical Affairs · Scientific Communications · MedOps AI Platform

Your extended Medical Affairs team.

Medical content, scientific communication and HCP education, developed by specialists and reviewed by qualified medical professionals, for pharmaceutical, biotechnology, medical device and life sciences companies.

Where do you need support?

A brand to supportMedical content, reviewed line by lineA product launchLaunch materials in every formatA publicationManuscripts, abstracts and postersA brief to deliverUpload it, get final deliverables
  • Qualified medical review on every piece
  • Every claim linked to its reference
  • Full version and decision history
  • Hyderabad · Mumbai · Dubai · Princeton
Since 2007Serving healthcare and pharma
100+Healthcare and pharma organisations
4 officesHyderabad · Mumbai · Dubai · Princeton
4 solutionsAlready used by pharma teams
Built for regulated work
  • UCPMP 2024
  • OPPI Code
  • IFPMA Code
  • DPDP Act 2023
  • GDPR
  • ISO/IEC 27001-aligned
  • Veeva PromoMats-ready
Trust and security
The challenge

Medical Affairs is more than medical content.

It connects scientific evidence, clinical practice and healthcare professionals. Many organisations find it hard to build and keep every capability that requires.

Limited capacity

Small in-house medical affairs and medical writing teams.

Rising content demand

More scientifically substantiated content across more brands.

Long review cycles

Several rounds across medical, regulatory and marketing teams.

Scattered approvals

Content, design and decisions spread across email and files.

HCP expectations

Growing demand for quality education and scientific engagement.

Fixed-cost pressure

Scaling quality without adding permanent headcount.

How medical content gets made

Watch a brief move through the team.

From the brand manager’s brief to released materials: evidence, writing, qualified medical review and design, with every step visible and every decision recorded.

  • You share the brief and the evidence that sets the limits
  • A qualified medical reviewer approves every line
  • Approved content is designed to your brand and released

See how we work

Brand manager shares the brief and approved references
Our platform

One workspace, from brief to release

Our Medical Affairs Workspace connects the brand team and the medical reviewer in one place. Every request shows its stage, owner and due date, so nothing waits in an inbox.

  • Brand managers raise requests and upload the evidence that sets the limits
  • Reviewers edit wording, add notes and comment on any line
  • Approve, request changes or reject, with every decision logged
  • Approved content moves straight to design, then to release
Medical Affairs Workspace · Medical review
The workspace review screen: a slide with highlighted statements and a panel of quality-check flags for the medical reviewer
Medical writers and reviewers working through materials togetherQualified medical review on every piece
Our team

Specialists behind every piece.

Each engagement is staffed by people who know the science and the rules it must follow.

Medical writers

Evidence-based content in every format

Medical reviewers

Qualified review of every claim

Designers

Production to your brand guidelines

Project leads

One accountable contact

Engagement

Support that fits your organisation

Not every organisation needs a full Medical Affairs department. Choose ongoing support, defined projects or specialist help when you need it.

For launches

Launch Kit

A coordinated set of scientific and brand materials for a new product, generic or biosimilar launch.

Per launch
For multi-brand teams

Brand Content Engine

Recurring content development and medical review with agreed monthly deliverables.

Monthly retainer
For growing companies

Medical Team on Demand

Medical writing, scientific content and qualified review without a full in-house team.

Per asset or monthly
For large organisations

Enterprise Services

Specialist content and operations support that fits your existing medical, regulatory and approval processes.

Custom scope

Who we work with

  • Indian pharmaceutical companies
  • Generic and specialty pharma
  • Biotechnology
  • Medical devices
  • Nutraceuticals
  • Life sciences
  • Global pharma organisations

Start with a conversation about your next launch or brand.

Four clear stages take you from discovery to your first released deliverables.