FORGE IQ™ · AI-Powered Industry Simulation Platform · Launching 1 June 2026
Practise the meeting. Become the writer.
You have learned medical writing. You have not yet lived it. FORGE IQ™ is the AI-powered simulation platform that places you inside 12 real pharmaceutical meetings, with multi-persona AI counterparts who respond in real time, and a Principal Medical Writer (Dr Elena Rossi) who authors a first-person debrief at the end of every session.
FORGE IQ™ Regulatory Track launches 1 June 2026. Founding Cohort is capped at 15 seats so every candidate receives full Principal Medical Writer critique attention. Pre-enrolment is open now at a founding-cohort rate of £1,799 (standard rate £1,999 from cohort 2 onwards). Pre-enrolment closes when the 15 seats are taken or on 31 May 2026, whichever comes first.
The experience-gap paradox FORGE IQ™ solves
The pharmaceutical industry has a structural training gap. Medical writing is one of the most well-paid, in-demand roles in pharma, yet candidates cannot get hired without "industry experience", and the only way to get industry experience is to be hired. Universities teach the theory. CROs teach the templates. Nobody teaches how to behave inside the meeting that sets up the document, and meetings are where regulatory writing careers are made or lost.
FORGE IQ™ is the platform that closes that loop. It places you inside 12 real industry meetings, under voice-driven pressure, with multi-persona AI counterparts who respond in real time and a Principal Medical Writer who critiques your performance in her own voice afterwards.
The 12 scenarios in the Regulatory Track
The Regulatory Track launching 1 June 2026 ships with 12 hand-authored meeting scenarios, each anchored to a distinct competency under pressure. No two overlap. Each scenario has 4 therapeutic-area variants (T2DM, oncology, rare disease, vaccines), giving you 48 unique simulation paths within the Regulatory Track alone.
Scenario 1
The New-Project Kick-Off Meeting
A novel compound's first KOM for CTD Module 2.7.4. Document scoping, study identification, pooling strategy, CV framing, timeline confirmation. The reference scenario for everything else.
Scenario 2
The Regulatory-Curveball KOM
A KOM in progress when a new agency request arrives mid-meeting. Tests adaptation under a moving target without losing structure.
Scenario 3
The Comment Resolution Meeting
You join a CR meeting on a 2.7.4 you didn't draft. The sponsor wants three changes that contradict the regulatory advice. Document defence under sponsor pressure.
Scenario 4
The Investigator's Brochure Update KOM
A new safety signal requires a mid-trial IB revision on a tight turn-around. Tests grasp of the IB structure and the regulatory cascade an update triggers.
Scenario 5
The TLF Inaccuracy Crisis Meeting
Biostatistics discovers a numerical error in a TLF you have already drafted from. Emergency meeting at week 12 of a 16-week timeline.
Scenario 6
The Late-Breaking Safety Signal Meeting
Mid-draft of an in-flight CSR, a new ADR is reported that may need adding to safety sections. Judgement on what to escalate, incorporate, and how.
Scenario 7
The Database Lock Delay Renegotiation
DB lock slips by 3 weeks. You rework the timeline, renegotiate with sponsor, communicate honestly. Difficult-conversation handling under deadline.
Scenario 8
The FDA Type B Meeting Preparation
Writing the briefing book in 5 days for a Type B interaction with FDA. Rapid-turnaround writing under defined regulatory etiquette.
Scenario 9
The Pre-Submission Expert Review
You defend a near-final document against internal QC and an expert reviewer who has just spotted 3 positioning concerns. Editorial discipline.
Scenario 10
The Oncology Accelerated Approval KOM
Single-arm study, ORR-driven, surrogate-endpoint reasoning, accelerated approval pathway. The differentiated language of oncology submissions.
Scenario 11
The Rare Disease Orphan Drug KOM
Small dataset, regulatory flexibility, accelerated and conditional approval pathways. Reasoning when conventional statistical power is absent.
Scenario 12
The Paediatric Investigation Plan Negotiation
EMA paediatric committee interaction, extrapolation argumentation, PIP commitments. A specialised regulatory dialogue most writers haven't encountered.
The personas you sit across from
Each meeting is performed in front of multi-persona AI counterparts with distinct voices, distinct knowledge, and distinct pressure. They reply in real time to what you say. Hand-authored personality, real industry conventions, no scripted answers.
Priya Nair
Regulatory Affairs Lead
Dr Adaeze Obi
Medical Director
Marcus Yuen
Biostatistician
Claire Donoghue
Project Manager
Dr Elena Rossi
Principal MW & QC Lead
The Dr Elena Rossi debrief — the FORGE IQ™ moat
Every session ends with a first-person debrief authored by Dr Elena Rossi, Principal Medical Writer and QC Lead. Not a peer. Not an algorithm scoring you against a rubric. A senior persona who watched the meeting and tells you, in flowing British English, what struck her about your performance.
The debrief follows seven sections: opening observation, what was handled well (two or three specific exchanges, named), verbatim upgrades (Dr Rossi quotes what you said, writes the sentence a senior would have used, and explains in one line why), the regulatory consequence of each critical gap (not "this is important" but "here is what happens to the document, when, and what it costs"), maturity-band placement, three concrete next-actions, and one sentence of closing encouragement.
To our knowledge, this is the only AI-generated post-simulation critique in medical writing that combines verbatim quote-and-upgrade, regulatory consequence reasoning, and explicit maturity placement.
The four-band maturity ladder
Every session is placed on a four-band maturity ladder. Your band is not a permanent rank, it is how you performed that day, in that scenario, in that mode. The platform tracks personal-best band per scenario over time. Certificates are awarded only at Proficient or higher.
Band 1
Foundation
First exposure. The senior is patient. You are learning the room.
Band 2
Practising
The instincts are forming. You ask several of the right questions without prompting.
Band 3
Proficient
Certificate awarded. You handled the meeting the way a senior medical writer would.
Band 4
Principal
Certificate awarded. You drove the meeting, anticipated the gaps, and led the room.
Three modes that grow with you
The platform recommends the next mode automatically based on your previous-session band. You can override. First-time users default to Coached.
Coached
On-screen cues per slide. Dr Rossi steps in once during the meeting to model a question you should have asked. For first sessions and confidence rebuilding.
Practising
Cues off. You are alone with the SMEs. Dr Rossi sits silently and writes the debrief afterwards.
Real
Cues off, plus industry curveballs: deadline shifts, data delays, sponsor changes. Closest to a live KOM.
The drafting exercise — closing the loop
A meeting only matters if it sets up a good document. After the debrief, FORGE IQ™ invites you into a drafting phase. You see a Reference Pack of real tabular safety data you would have at the start of writing (pooled TEAEs, adjudicated MACE, hepatic abnormalities, exposure summaries), with an explicit flag listing the tables that are not yet available so your draft must reflect that constraint honestly.
You write 120 to 180 words of the document opening. Dr Rossi critiques against six criteria: regulatory tone, accurate pooling, precise CV framing language, transparent hepatic reporting, structure, and citation accuracy. She quotes your phrases verbatim and rewrites one or two in senior phrasing.
This is the only way to test whether you can translate a meeting into the act of writing, which is the job.
Who FORGE IQ™ is built for
FORGE IQ™ is not an entry-level medical writing course. It assumes you can already draft regulatory documents. It is built for three specific moments in a medical writing career.
Audience 1
The transitioning clinician or aspiring medical writer
You are a doctor, pharmacist, nurse, biomedical scientist or science graduate moving into regulatory medical writing. You have read the guidelines. You have written practice essays. You have never been the medical writer in a room with senior SMEs looking at you, expecting professional, leading, regulatory-aware questioning.
FORGE IQ™ closes that gap before your first real KOM, not after.
Audience 2
The junior medical writer in role (0 to 2 years)
You got hired. You are surviving. You can write the documents. But you freeze in cross-functional meetings, sponsor calls and stakeholder reviews. The senior writers in your team seem composed in those moments and you cannot work out how. PharmaLink Regulatory Medical Writing graduates receive the Alumni Continuation Rate.
Audience 3
The B2B L&D buyer
You run a CRO, a sponsor team or a medical communications agency. You hired smart junior writers. They can draft. They freeze in client meetings and your senior writers are spending billable hours mentoring them. FORGE IQ™ ships those juniors through the room-readiness scenarios at scale, on a per-seat annual licence.
What you walk away with
- A maturity profile across 12 scenarios. Personal-best band per scenario, tracked over time. The platform remembers your previous sessions and recommends the next mode automatically.
- A LinkedIn-shareable certificate at Proficient or Principal band. The certificate states the specific scenario and the band achieved. Defensible, not a participation prize. "FORGE IQ™ — The Comment Resolution Meeting — Proficient (PharmaLink Academy)" is a signal a hiring manager understands.
- A library of completed scenarios you can discuss in interview. Kick-off meeting, comment resolution, IB update, TLF crisis, safety signal, database delay, FDA Type B prep, expert review, oncology accelerated approval, rare disease, paediatric negotiation, regulatory curveball. Each is a story you can tell.
- The vocabulary and judgement of a senior medical writer. Not because you watched senior writers operate, but because you operated alongside Dr Rossi and four AI senior SMEs, in the room, with feedback, repeatedly.
Why I built FORGE IQ™
I am Dorothy Ogwuru. I spent 18 years in pharmacovigilance and regulatory medical writing across Schering-Plough, MSD, Amgen, Takeda and Tillomed as Global Head of Pharmacovigilance during COVID. My RMW track started at Roche in 2013, then AstraZeneca, GSK as Senior Regulatory Medical Writer, the Novo Nordisk Ozempic submission, and Daiichi Sankyo.
Across all of that, I have watched, mentored and hired junior medical writers. The single most consistent gap I have observed is not in their writing. It is in their ability to operate inside the room when the writing is contested. They have learned the craft. They have not lived the scenarios. That gap took them 3 to 7 years to close the slow way. FORGE IQ™ is what I built to close it inside a structured programme.
I designed the platform architecture, the 12 signature scenarios, the persona system and the Dr Rossi assessment rubric. I retain editorial ownership of every scenario and every debrief criterion. The platform is delivered by Dr Elena Rossi, the AI Principal Medical Writer persona, operating to the standard I would apply on a real document team.
FORGE IQ™ pricing
FORGE IQ™ is sold as a standalone simulation platform. PharmaLink RMW graduates receive an alumni continuation rate, available post-graduation. Institutional buyers are priced per seat with volume tiers.
B2C · Founding Cohort
FORGE IQ™
Founding Cohort rate. Reverts to £1,999 from cohort 2. 15 seats only. Closes 31 May 2026 or when full.
- All 12 signature scenarios across 4 therapeutic variants
- Dr Rossi debriefs after every session
- Maturity band tracking and certificates at Proficient and above
- Browser-based, voice-driven, 25 minutes per scenario
- For aspiring medical writers, junior MWs and transitioning clinicians
PharmaLink RMW Alumni
FORGE IQ™ Continuation Rate
Available post-graduation only. Continuing professional development pathway.
- All 12 signature scenarios across 4 therapeutic variants
- Dr Rossi debriefs after every session
- Maturity band tracking and certificates at Proficient and above
- Alumni rate verified via PharmaLink RMW completion
B2B · Per Seat
FORGE IQ™ for Teams
Per seat. Annual licence. Volume tiers from 5 seats.
- 5+ seats at £2,099 per seat
- 15+ seats at £1,799 per seat
- L&D reporting on team-level maturity progression
- Defensible audit trail of competency by scenario
- For CROs, sponsor teams, medical communications agencies
Frequently asked questions
Is FORGE IQ™ a course?
No. There is no video to watch, no quiz to tick. FORGE IQ™ is a voice-driven AI simulation platform. You enter a virtual conference room, hold down a microphone button, and have a 25-minute conversation with multi-persona AI counterparts in distinct realistic voices. At the end, Dr Elena Rossi (Principal Medical Writer persona) authors a first-person debrief. If you need to learn medical writing from zero, the PharmaLink Regulatory Medical Writing programme is the entry path.
Who is Dr Elena Rossi?
Dr Elena Rossi is the Principal Medical Writer and QC Lead persona who authors the debrief at the end of every FORGE IQ™ session. She is voiced in flowing British English. Her critique follows a strict 7-section format: opening observation, what was handled well, verbatim upgrades, regulatory consequences of gaps, maturity band placement, three concrete next-actions, and closing encouragement. Her assessment rubric was designed by Dorothy Ogwuru and reflects the standard a real Principal MW would apply on a regulated document team.
Is this just a ChatGPT wrapper?
No. FORGE IQ™ runs on Anthropic Claude Sonnet 4.6 with OpenAI Text-to-Speech, both server-side with PharmaLink controlling the keys. Persona-specific system prompts are grounded in real ICH guidance, EMA scientific advice patterns, FDA conventions and pharmaceutical industry practice. Personas stay in character. Scenarios are hand-authored. Dr Rossi's critique follows a strict assessment rubric. This is a designed, performed simulation with measurable outputs, not a wrapper around a general chatbot.
How long does each session take?
Each meeting is approximately 25 minutes voice-driven, followed by the Dr Rossi debrief and the optional drafting exercise of 120 to 180 words. Most candidates complete one scenario per sitting and return to repeat scenarios at different bands across the Founding Cohort window.
When does FORGE IQ™ launch and how do I reserve a seat?
FORGE IQ™ launches on 1 June 2026 with the Regulatory Track. The Founding Cohort is capped at 15 seats. Pre-enrolment is open now at a founding-cohort rate of £1,799 (standard rate is £1,999 from cohort 2 onwards). Pre-enrolment closes when the 15 seats are taken or on 31 May 2026, whichever comes first. Enrol directly above, or book a fit call to discuss.
What does the certificate actually say?
The certificate is a downloadable HTML document in PharmaLink Consultancy livery, signed by Dr Elena Rossi, citing the specific scenario, the date, the mode (Coached, Practising, or Real) and the band achieved (Proficient or Principal). Designed to be printed to PDF or shared on LinkedIn. The certificate names the scenario explicitly; it is not a participation prize.
What is the alumni rate eligibility?
The PharmaLink RMW Alumni Continuation Rate is available to graduates of the PharmaLink Regulatory Medical Writing programme. Eligibility is verified at enrolment. The rate is available post-graduation, not as part of an RMW package. FORGE IQ™ is sold as a standalone platform; the alumni rate reflects continuing professional development, not a bundle discount.
How does the B2B per-seat licence work?
Institutional buyers purchase annual seats. Each seat gives one team member full access to the FORGE IQ™ platform, including all 12 scenarios, all 4 therapeutic variants, Dr Rossi debriefs and the maturity profile. Per-seat pricing decreases with volume. L&D leads receive reporting on team-level maturity progression by scenario, plus a defensible audit trail of competency. Per-seat agreements include implementation support from Dorothy.
You don't need another course. You need 12 real meetings before your first real one.
FORGE IQ™ launches 1 June 2026 with 15 Founding Cohort seats at £1,799 (standard rate £1,999 from cohort 2). Enrolment closes when the 15 seats are taken or on 31 May 2026, whichever comes first. Junior medical writers, transitioning clinicians and recent RMW graduates enrol directly. L&D buyers for industry teams should request the institutional brief.
Enrol in the Founding Cohort →