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Seeding KOLs for a Clinical Product: Advisory Boards Under NMC Conduct Rules

How to structure a clinical advisory board and fees for a healthcare product in India without breaching the conduct rules on gifts, hospitality and endorsement.

Seeding KOLs for a Clinical Product: Advisory Boards Under NMC Conduct Rules

This post is for healthtech founders, medical affairs leads and marketers who plan to build a clinical advisory board around a product aimed at doctors. It is also for the doctors who are asked to join one and want to know what they can and cannot accept.

The question it answers: how do you structure advisory roles, honoraria and related activity so that the arrangement stands up against the conduct rules that apply to Indian doctors? This is a framework for discussion with your lawyer, not legal advice, and it does not tell any doctor what they may do. The rules are written for doctors; the company designing the programme should work inside the same limits, because a doctor who breaches them is the one who faces the penalty.

A note on sources. The conduct provisions discussed here come from the Indian Medical Council (Professional Conduct, Etiquette and Ethics) Regulations, 2002, as amended and published on the National Medical Commission website. The NMC has since issued other documents on professional conduct and advertising. Ask your counsel to confirm which text governs the specific activity before you finalise any contract.

Why advisory boards attract scrutiny

An advisory board has legitimate purposes: getting clinical input on a product, testing workflows, shaping a clinical roadmap and building credibility with clinicians. It also has an obvious risk. Payments and perks to prescribers or referrers can look like inducements. For that reason the regulations separate real professional work from benefits that could influence clinical judgement.

For healthtech, one more point applies. The regulations refer to the "pharmaceutical and allied health sector industry". A health software or device company is likely to be treated as part of the allied health sector for this purpose, although that reading is for your counsel to confirm. Plan as if it applies.

What the regulations say

Clause 6.8.1 of the 2002 Regulations sets out the stipulations. In summary:

  • Gifts: a medical practitioner shall not receive any gift from the industry or its representatives.
  • Travel: a practitioner shall not accept travel facilities, including rail, road, air, ship, cruise tickets or paid vacations, from the industry for self and family for vacation or for attending conferences, seminars, workshops or CME programmes as a delegate.
  • Hospitality: a practitioner shall not accept individually hospitality such as hotel accommodation for self and family under any pretext.
  • Cash or monetary grants: a practitioner shall not receive any cash or monetary grants from the industry for individual purpose in individual capacity under any pretext. Funding for research and study can be received only through approved institutions, transparently and with full disclosure.
  • Research: industry-funded research is permitted if specified conditions are met, including competent authority permission, ethics committee clearance, public disclosure of funding source and amount and the freedom to publish results.
  • Autonomy: professional autonomy and the autonomy of the institution must never be compromised.
  • Affiliation: a practitioner may work for the industry in advisory capacities, as consultants, researchers or treating doctors, provided professional integrity and freedom are maintained, patients' interests are not compromised, the affiliation is within the law and the affiliation is fully transparent and disclosed.
  • Endorsement: a practitioner shall not endorse any drug or product of the industry publicly. Studies on efficacy should be presented through appropriate scientific bodies or published in appropriate journals.

The same document sets graded actions for violations. For gifts, for example, the action scales from censure for small amounts up to removal from the medical register for periods that lengthen with the amount. Treat the penalty ladder as a reason to be conservative.

Separately, clause 6.4.1 prohibits a practitioner from giving, soliciting or receiving any gift, gratuity, commission or bonus in return for referring, recommending or procuring any patient. An advisory arrangement must never be, or look like, a reward for referrals or usage.

Two clauses in tension, and how to read them

Notice the apparent tension. Clause 6.8.1(d) bars cash "for individual purpose in individual capacity under any pretext", while 6.8.1(g) explicitly permits advisory and consulting work. A sensible reading, to be tested with counsel, is that fair payment for genuine, documented professional work done under a written agreement and fully disclosed is different from a grant or gift to the individual. A payment that is not tied to defined work, or that rises with prescribing or purchasing, falls on the wrong side of that line.

Do not rely on that reading alone. Ask counsel how the doctor's employer, hospital and state medical council view it, and whether the hospital needs to approve the engagement.

Designing the board

A defensible structure has these features.

A real need. Write down what you need advice on, before you pick names. If you cannot describe the work in two sentences, you do not yet have a board.

A defined number of advisers. Choose the smallest group that covers the expertise. A large board with thin duties looks like a reward scheme.

Selection by criteria, not by sales potential. Pick on expertise, independence and availability. Record the criteria. Do not choose advisers because they are large prescribers or purchasers, and keep the commercial team out of selection.

A written agreement per adviser. It should cover the scope of services, the number of meetings and deliverables, the term, the fee basis, expense rules, confidentiality, intellectual property, disclosure obligations and termination. It should say that the adviser keeps professional independence and that nothing obliges the adviser to use, recommend or refer the product.

Fair fees tied to time. Set a rate by reference to the time and expertise needed, apply it consistently, and pay for work done and documented. Avoid fees linked to the number of users, patients, prescriptions or purchases. Avoid bonuses of any kind.

Meetings that are meetings. Hold sessions where real work happens, with agendas and minutes. Choose a venue suited to the work, not a leisure setting, and keep hospitality modest. Do not fund travel for family members.

Disclosure. Agree that the adviser will disclose the affiliation to their employer, patients where relevant and any audience when speaking about the product. Keep a register of advisers and fees and be ready to share it on request.

A firewall from sales. The commercial team should not influence the board's recommendations, and advisers should not receive sales targets or product usage reports.

What not to do

  • Do not offer gifts, even small ones. The clause is not limited by value, and the penalty ladder starts at small amounts.
  • Do not pay for a doctor to attend a conference as a delegate.
  • Do not ask an adviser to post about the product, appear in your advertising or lend their image or voice. Our summary of the 2026 NMC advertising guidelines explains why doctors cannot be used to promote products, and the NMC compliance handbook goes further.
  • Do not link any benefit to referrals, prescribing or purchases.
  • Do not run a "KOL" programme as a disguised sales channel.
  • Do not offer cash grants to individuals in the name of research. Route research funding through an approved institution.

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A decision table for common requests

These are hypothetical requests an adviser or a company might raise. The right-hand column is a conservative starting position for discussion with counsel, not a ruling.

RequestConservative position
A flat fee for four two-hour review sessions, paid on a signed timesheetDefensible if scope, rate and disclosure are written down
A gift hamper at a festivalAvoid. Gifts are barred
Business-class flights and a resort stay for an adviser and spouseAvoid. Travel and hospitality for family are barred
Reimbursement of economy travel and a night's stay for an in-person working sessionDiscuss with counsel; keep modest, documented and limited to the adviser
A bonus when the adviser's department adopts the productAvoid. This links reward to use
Funding an investigator-led study through the hospital's research officeDefensible if ethics approval, disclosure and publication rights are in place
A named adviser quoted in your brochure as endorsing the productAvoid. Public endorsement is barred
A thank-you cash payment after a successful pilotAvoid. It is a payment without defined work

A hypothetical board

Consider a hypothetical startup building a tool for post-operative follow-up in orthopaedics. It identifies four needs: clinical workflow review, patient-instruction content review, outcome-measure selection and evaluation design for a later study. It recruits three orthopaedic surgeons and one physiotherapist, chosen from different cities and care settings, using written criteria. Each signs a twelve-month agreement for quarterly working sessions, with a time-based fee set before any session. The surgeons' hospitals are informed. The company's sales team does not attend. Minutes record advice given and what the company did with it.

Nothing in that arrangement involves a gift, a trip for family, a link to referrals or a public endorsement. That is the aim, not the fee level.

KOL marketing without the risk

The term KOL is common in industry, but a better frame is "clinical adviser" or "scientific adviser". The valuable parts of such a relationship are advice, co-development, independent evidence and education delivered through proper scientific channels.

There are compliant ways to build clinical credibility:

  • Support independent, ethics-approved studies run through institutions, with publication rights preserved.
  • Present evidence at scientific meetings and in journals, with disclosures.
  • Publish clinical rationale and methodology on your own site, reviewed by qualified clinicians.
  • Invite advisers to review content and give feedback, with their names used only where permitted and disclosed.

Our KOL marketing service page and KOL glossary entry describe the wider practice.

A review checklist

Before signing any adviser agreement:

  1. Is there a documented clinical need?
  2. Were advisers selected on criteria, by someone outside sales?
  3. Does the contract state scope, deliverables, fees and independence?
  4. Is the fee based on time and expertise, with no link to use or referrals?
  5. Are travel and hospitality limited to what the work needs, with nothing for family?
  6. Is disclosure built into the agreement?
  7. Has counsel reviewed it against the current NMC text and the doctor's institutional rules?
  8. Is there a register and a review date?

Where to start

Write the one-page need statement and the selection criteria before you contact any doctor. Show both to your lawyer first. If you want help building compliant clinical credibility around a product, our healthcare startup marketing work is a starting point.

Filed underkol seeding healthcare product indiaclinical advisory board indiaNMC rules doctor consultancy honorariumdoctor advisory board healthtechkol marketing compliance india

About the author

Founder & CEO · Gurugram, India

Nishu founded Branding Pioneers in 2016 with one rule that hasn't changed since: healthcare only. She'd run digital strategy at a top-10 Indian agency and watched generalist marketing underserve medical clients who needed something built for how patients actually search and decide. So she left to build the specialist instead. It's now an 80-person team working with healthcare brands worldwide.

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