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  • Driven by Evidence

Science with Integrity. Evidence with Impact.

In value-based healthcare, Medical Affairs is where a brand earns its credibility.

We connect clinical data to real-world outcomes so your therapy earns the trust of prescribers, payers, and patients.

Partner with Our Experts
  • Medical Affairs: Proof, Not Just Promise

Academic Evidence and Clinical Certifications

The Challenge:

High content volume led to superficial engagement metrics, making it hard for brands to share scientific data without seeming commercially biased.

Our Solution:

We partnered with an academic hospital to create a neutral certification engine focused on measurable clinical competence rather than vanity clicks.

15K+

HCPs Certified

>90%

Relevance Score

100%

Brand-Safe Awareness

Tier-1

Academic Partnership

Comprehensive Medical Affairs Services

Here are the core medical affairs capabilities we bring to your brand:

Real-World Evidence (RWE) Studies

  • We design observational studies and patient registries that capture long-term safety signals and treatment outcomes in routine clinical settings.
  • Our dual-evidence strategy combines Real-World Data (RWD) with clinical trial findings to answer the questions payers and HTA bodies ask before approving formulary access.
  • RWE protocol writing and claims data analytics give you the economic justification your brand needs to hold its market access position over time.
Design RWE Studies & Registries

Strategic Publication Planning

  • We build multi-year publication plans that construct your scientific evidence base milestone by milestone, from Phase 3 readouts to post-marketing data.
  • Our team handles manuscript authorship, journal targeting, and peer review navigation so your clinical findings reach the right audiences with impact.
  • Every publication we produce aligns with ICMJE authorship standards and global transparency disclosure requirements, protecting your brand’s scientific credibility.
Start Medical Publication Planning

KOL Advisory Boards

  • We structure advisory boards that give your top clinical experts a meaningful role in shaping medical strategy, label refinement, and trial design direction.
  • Our team handles logistics, compliance, and fair market value frameworks across a verified network of 500+ global experts spanning 35 countries.
  • Every advisory session produces structured intelligence your team can use to inform lifecycle management, publication strategy, and next-cycle evidence planning.
Organize KOL Advisory Boards

Scientific Symposia Management

  • We plan and execute symposia that position your brand as the leading scientific voice in its therapy area, both at congresses and as standalone events.
  • Abstract strategy, faculty coordination, and presentation development all sit with our team so your scientific leadership shows up consistently on the day.
  • Post-symposium content goes out through digital channels and medical publications so the scientific momentum you build at the event keeps working after it ends.
Manage Scientific Symposia

Medical Education (CME/CPD)

  • We develop accredited CME and CPD programs across live webinars, in-clinic modules, and digital learning pathways, reaching over 15,000 enrolled HCPs.
  • Clinical case simulations within disease education programs sharpen diagnostic accuracy and give prescribers the confidence to act earlier in the patient journey.
  • We take post-graduate education to Tier-2 and Tier-3 cities where brand advocacy forms at the precise moment young doctors develop their clinical habits.
Develop Accredited CME Programs

Post-Graduate Doctor Education

  • We design education programs for residents and post-graduate fellows at the stage where clinical patterns take root and prescribing preferences begin to form.
  • Modular, evidence-based content runs through our Next-Gen LMS and scales from a single hospital to a national multi-specialty rollout without losing quality.
  • Partnerships with medical associations including the Association of Otolaryngologists of India (AOI) give our programs accredited institutional reach across the country.
Build Post-Graduate HCP Education

Regulatory & Ethics Compliance

  • We audit all medical communications assets against FDA OPDP, EFPIA, and UCPMP standards so your brand stays compliant across every market it operates in.
  • Our compliance training programs give Medical Affairs teams clear, practical SOPs they can apply across promotional and non-promotional channels alike.
  • IRB submissions, ethics board navigation, and transparency disclosure reporting for investigator-sponsored studies are fully handled by our regulatory team.
Audit Medical Communications Compliance

Medical Information (MedInfo)

  • We run a compliant, 24/7 medical information response service that handles HCP and patient enquiries across phone, email, and digital channels.
  • MERLIN AI, our RAG-based pharma-specific language model, answers queries using only verified sources from PubMed, peer-reviewed journals, and authorised internal databases.
  • Air-gapped security architecture and mandatory audit trails mean no query data touches public AI models and every response stays within your compliance framework.
Deploy Pharma MedInfo Services

Health Economics & Outcomes Research (HEOR)

  • We build HEOR packages that include budget impact models, cost-effectiveness analyses, and quality-of-life data to give payers a compelling economic case.
  • Patient-Reported Outcome studies and indirect treatment comparisons give Health Technology Assessment bodies the comparative evidence they need for formulary decisions.
  • We translate HEOR findings into payer-facing value dossiers written specifically for formulary committees across India, Southeast Asia, and European markets.
Build HEOR Evidence Packages

Real-World Evidence (RWE) Studies

  • OneAlphaMed designs observational studies and patient registries to capture long-term safety signals and treatment outcomes in routine clinical settings.
  • The firm’s dual-evidence strategy synthesizes Real-World Data (RWD) to prove effectiveness beyond idealized Phase 3 conditions.
  • Rigorous RWE protocol writing and RWD analytics utilize claims data and patient-reported outcomes to justify broad market access.
Design RWE Studies & Registries

Strategic Publication Planning

  • Transforms clinical study reports into credible, peer-reviewed scientific narratives shaping clinical practice.
  • Medical writing ensures strict adherence to Good Publication Practice (GPP4) and ICMJE guidelines.
  • Executes an omnichannel strategy with visual abstracts, interactive supplements, and Plain Language Summaries.
Start Medical Publication Planning

KOL Advisory Boards

  • Captures the “voice of the expert” through structured scientific inquiries to stress-test brand assumptions.
  • End-to-end facilitation ensures balanced, unbiased peer-to-peer discussion.
  • Deploys secure Asynchronous Advisory Boards for deep data review over several days, reducing groupthink.
Organize KOL Advisory Boards

Scientific Symposia Management

  • Orchestrates high-profile medical congress events with rigorous scientific agenda development.
  • Omnichannel Congress Strategy executes seamless hybrid medical events with global reach.
  • Integrates AR/VR scientific posters and immersive data visualizations for interactive learning.
Manage Scientific Symposia

Medical Education (CME/CPD)

  • Specializes in CME content designed to shift clinical behavior and improve patient outcomes.
  • Accredited programs are grounded in formal needs assessment and Moore’s outcome levels.
  • Delivers interactive cases challenging HCPs with highly realistic, branching-logic patient scenarios.
Develop Accredited CME Programs

Post-Graduate Doctor Education

  • Cultivates the KOL pipeline by engaging residents when treatment habits are formed.
  • Delivers hands-on, hospital-based workshops on evidence-based practice and advanced diagnostics.
  • Utilizes digitized case studies that transform static records into interactive pathology visualizations.
Build Post-Graduate HCP Education

Regulatory & Ethics Compliance

  • Proactive Pharma Marketing Compliance Consulting builds a culture of zero variance.
  • AI-Driven MLR Review uses NLP to pre-screen promotional materials and reduce review cycles.
  • Ensures strict adherence to global/regional standards: FDA OPDP, EFPIA, and UCPMP.
Audit Medical Communications Compliance

Medical Information (MedInfo)

  • Builds sophisticated MedInfo ecosystems serving as the evidence-based source of truth.
  • Develops comprehensive Standard Response Letter (SRL) libraries and FAQs via vigilant literature monitoring.
  • Deploys AI Medical Information Systems and chatbots for seamless 24/7 omnichannel responses.
Deploy Pharma MedInfo Services

Health Economics & Outcomes Research (HEOR)

  • Translates clinical efficacy into financial utility, proving therapies are cost-effective investments.
  • Synthesizes clinical and humanistic evidence into comprehensive Global Value Dossiers.
  • Develops rigorous budget impact models and cost-effectiveness analyses for drug adoption projections.
Build HEOR Evidence Packages

The OneAlphaMed Approach

Evidence-Based Medical Communication: We take real-world evidence, clinical data, and clinic-floor conversations and turn them into credible medical communication that healthcare professionals actually use in prescribing and patient management.

  • Common Questions

Frequently Asked Questions

Common inquiries from Medical Affairs leaders regarding our methodologies:

We utilize advanced AI-driven Medical Legal Regulatory (MLR) review systems and employ compliance experts well-versed in FDA OPDP, EFPIA code compliance, and UCPMP guidelines. This ensures that cross-border HCP engagement rules and pharmacovigilance standards are strictly maintained at all times.

We focus on bridging the gap between clinical data and real-world outcomes. From RWE protocol writing to claims data analysis, we leverage global datasets and Real-World Data (RWD) India to execute non-interventional studies that prove true effectiveness beyond controlled trials.

We offer highly flexible Medical Education solutions. Depending on your brand’s strategic needs, we provide unbranded medical education, interactive clinical cases, and accredited CME programs that can be executed both with or without specific institutional endorsements.

  • Let's Talk

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We get back quickly and point you to exactly the right solution.

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