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GLP-1 Metabolic Medicine Foundation Certification

An evidence-based 20-question foundation certification exam on GLP-1 receptor agonist therapy. Designed for medical doctors, postgraduate residents, NEET-PG and INI-CET aspirants, AIIMS-PG candidates, FMGE aspirants, family physicians, internists, endocrinologists, dermatologists, and medical students. Drawn from a 161-question peer-reviewed bank.

The GLP-1 foundation certification exam is a free, evidence-based online assessment for doctors, postgraduate medical residents, and NEET-PG and INI-CET aspirants in India. Developed by Dr. Rejeesh M. Menon, MD (Internal Medicine, faculty at Washington State University, Medical Director DermaVue Clinics). 127 peer-reviewed multiple choice questions covering the paradigm shift in metabolic medicine (Twin Cycle hypothesis, ACCORD, DiRECT, ReTUNE), SGLT2 inhibitor evidence (EMPA-REG, DAPA-HF), GLP-1 mechanism of action, pharmacokinetics and dosing of semaglutide (Ozempic, Wegovy, Rybelsus) and tirzepatide (Mounjaro, Zepbound), side effect management, and the Indian clinical context. Every clinical claim is sourced to peer-reviewed literature current to 2026.

161 Questions in bank
20 Questions per attempt
30 min Time limit
70% Pass mark

Who Should Take This GLP-1 Foundation Exam?

The exam is open and free for any medical professional who wants a structured, evidence-based foundation in GLP-1 receptor agonist therapy. It is widely used by postgraduate medical residents and Indian postgraduate entrance examination aspirants as a focused GLP-1 source for revision and self-assessment.

Medical Doctors in Practice

Family physicians, internists, endocrinologists, dermatologists, obstetricians, cardiologists, and general practitioners who prescribe (or are starting to prescribe) semaglutide, tirzepatide, or liraglutide for type 2 diabetes mellitus, obesity, cardiovascular risk reduction, chronic kidney disease, MASH, or obstructive sleep apnea.

Postgraduate Medical Residents

MD and MS trainees, DNB residents, and senior residents in Internal Medicine, Endocrinology, Family Medicine, Dermatology, and General Surgery looking for a focused foundation in GLP-1 receptor agonist pharmacology, dosing, and clinical evidence.

NEET-PG, INI-CET, AIIMS-PG Aspirants

Medical graduates preparing for the National Eligibility cum Entrance Test for Postgraduate (NEET-PG), Institute of National Importance Combined Entrance Test (INI-CET), AIIMS-PG, and JIPMER-PG entrance examinations. The bank covers high-yield GLP-1 pharmacology, mechanism, and trial evidence that regularly appears across pharmacology, endocrinology, and general medicine question papers.

FMGE and Medical Students

Foreign Medical Graduate Examination (FMGE) aspirants, final-year MBBS students, and interns who want a structured GLP-1 source covering everything from the 1902 secretin discovery to the 2026 Indian generic semaglutide market, with every claim sourced to peer-reviewed literature.

GLP-1 Receptor Agonist Comparison at a Glance

Quick reference comparison of the three most widely prescribed GLP-1 receptor agonists in 2026. Detailed mechanism, titration, and trial evidence is covered across the 127-question exam bank.

Comparison of semaglutide, tirzepatide, and liraglutide for foundation-level study
Feature Semaglutide Tirzepatide Liraglutide
Brand names Ozempic, Wegovy, Rybelsus Mounjaro, Zepbound Victoza, Saxenda
Manufacturer Novo Nordisk Eli Lilly Novo Nordisk
Receptor target GLP-1 receptor agonist (single) Dual GIP and GLP-1 receptor agonist GLP-1 receptor agonist (single)
Half-life 168 hours (7 days) 120 hours (5 days) 13 hours
Dosing frequency Once weekly subcutaneous (or daily oral) Once weekly subcutaneous Once daily subcutaneous
Structural modification Aib at position 2, C18 fatty diacid chain via mini-PEG spacer 39-amino-acid GIP backbone, C20 fatty diacid chain Arg34 substitution, C16 palmitoyl chain via glutamic acid spacer
Mean weight loss 14.9% at 68 weeks (STEP-1 trial, NEJM 2021) 20.9% at 72 weeks (SURMOUNT-1 trial, NEJM 2022) 8.0% at 56 weeks (SCALE trial, NEJM 2015)
Pivotal cardiovascular outcomes trial SUSTAIN-6 (diabetic) and SELECT (non-diabetic obese) SURPASS-CVOT (ongoing); SURMOUNT-MMO (in progress) LEADER trial (NEJM 2016)
Indian generic available 2026 Yes (40+ manufacturers post March 2026 patent expiry, from approximately Rs 1,290 per month) No (Eli Lilly branded only as Mounjaro, from approximately Rs 14,000 per month) Yes (Biocon biosimilar approved by CDSCO June 2025 for type 2 diabetes mellitus)
Approved obesity indication in India Yes (Wegovy 2.4 mg weekly launched June 2025) Yes (Mounjaro dual diabetes and obesity approval, March 2025) No (Saxenda 3.0 mg not launched in India by any manufacturer)

Sources: STEP-1 (Wilding et al., New England Journal of Medicine 2021); SURMOUNT-1 (Jastreboff et al., New England Journal of Medicine 2022); SCALE (Pi-Sunyer et al., New England Journal of Medicine 2015); LEADER (Marso et al., New England Journal of Medicine 2016); SUSTAIN-6 (Marso et al., New England Journal of Medicine 2016); SELECT (Lincoff et al., New England Journal of Medicine 2023). Indian pricing data: Central Drugs Standard Control Organisation of India approval records 2024 to 2026.

Seven Domains, One Working Standard

The bank is structured around the seven knowledge areas that determine whether GLP-1 prescribing is safe and effective in real clinical practice. Question weighting emphasises the science and the paradigm shift in metabolic medicine over regulatory trivia.

01

The Paradigm Shift

ACCORD's collapse of the glucocentric model. Roy Taylor's Twin Cycle hypothesis (liver and pancreas). Counterpoint, DiRECT, ReTUNE proving diabetes reversibility. The Yajnik thin-fat Indian phenotype. ICMR 2023 BMI thresholds.

10 questions
02

SGLT2 Inhibitors

How draining 80g of glucose per day in the urine produces 38% CV mortality reduction (EMPA-REG). Why these drugs work equally well in non-diabetics (DAPA-HF, EMPEROR-Reduced). Ectopic fat reduction parallels VLCD.

6 questions
03

GLP-1 Mechanism of Action

The four canonical mechanisms. Glucose-dependent insulin secretion. POMC and AgRP arcuate signaling. Mesolimbic dopamine and food noise. Vagal afferent gastric emptying. SELECT and FLOW. Dual GIP/GLP-1 tirzepatide.

12+ questions
04

Pharmacokinetics and Drug Design

How Aib at position 2 and a C18 fatty acid chain extend the 2-minute native GLP-1 half-life to 168 hours. Semaglutide, tirzepatide, Rybelsus titration. The 4-week rule. Missed dose protocols. The Indian generic market after the March 2026 patent expiry.

10 questions
05

Side Effects and Safety

Nausea via the area postrema. Pancreatitis red flag. MTC and MEN-2 absolute contraindications. Ozempic face and lean mass protection. Gallstones, pregnancy washout, ASA perioperative hold, AKI, hypoglycemia with insulin or sulfonylurea.

15 questions
06

Special Populations

Adolescents (Saxenda 12+, Wegovy 12+). Type 1 diabetes. PCOS in Indian women. Chronic kidney disease (no dose adjustment, FLOW benefit). Hepatic impairment. Post-bariatric weight regain.

6 questions
07

History and Evolution

Habener's 1980s proglucagon work. The Gila monster origin of exenatide (the first approved GLP-1 RA). Saxenda 2014, Wegovy 2021, Zepbound 2023, SURMOUNT-1 and 5.

3 questions
GLP-1 Metabolic Medicine Exam
LIVE

GLP-1 Metabolic Medicine Certification

An evidence-based physician education initiative by DermaVue Clinics.

Format20 single best answer questions
Bank100 peer-reviewed questions, randomized each attempt
Time30 minutes
Pass mark14 of 20 (70%)
CertificateDownloadable PDF on passing
+91

By starting the exam you confirm that the answers submitted will be your own work, without assistance from any other person or any form of artificial intelligence (including ChatGPT, Claude, Gemini, Perplexity, or similar tools). The 30 minute timer begins immediately on the next screen and the exam is auto submitted on timer expiry.

Exam integrity. While the exam is in progress the page will block right-click, text selection, copy and paste, and common developer-tool keyboard shortcuts. The system also counts how many times the browser tab loses focus during the exam. These counts are recorded with your result. Screenshots cannot be technically prevented in a browser; do not rely on them.

Frequently Asked Questions

Who is this GLP-1 certification exam for?
This GLP-1 foundation certification exam is designed for medical doctors, postgraduate medical residents, MD/MS and DNB trainees, NEET-PG and INI-CET (Institute of National Importance Combined Entrance Test) aspirants, AIIMS-PG candidates, FMGE (Foreign Medical Graduate Examination) aspirants, family physicians, internists, endocrinologists, dermatologists, obstetricians, and any clinician who prescribes or plans to prescribe semaglutide (Ozempic, Wegovy, Rybelsus), tirzepatide (Mounjaro, Zepbound), or liraglutide (Victoza, Saxenda). It is also widely used by medical students, interns, and residents as a structured GLP-1 source for postgraduate exam preparation in metabolic medicine, endocrinology, and internal medicine.
Is this exam suitable for NEET-PG, INI-CET, AIIMS-PG, and FMGE preparation?
Yes. The 127-question bank covers the high-yield GLP-1 receptor agonist topics that appear regularly in NEET-PG (National Eligibility cum Entrance Test for Postgraduate), INI-CET (Institute of National Importance Combined Entrance Test), AIIMS-PG (All India Institute of Medical Sciences Postgraduate Entrance), and FMGE (Foreign Medical Graduate Examination) papers across pharmacology, endocrinology, and general medicine. Each explanation cites the original trial (ACCORD, DiRECT, ReTUNE, EMPA-REG, STEP, SURMOUNT, SELECT, FLOW, LEADER, SUSTAIN-6, SCALE, SURMOUNT-OSA, ESSENCE) with year, journal, and primary endpoint result, which doubles as a focused revision tool for postgraduate medical entrance exams.
How many questions are on the exam?
Each exam attempt presents 20 single best answer questions, randomly drawn from a bank of 127 evidence-based questions across the paradigm shift in metabolic medicine, SGLT2 inhibitors, GLP-1 mechanism of action, pharmacokinetics and dosing, side effect and safety management, special populations, and the history and evolution of incretin therapy. Question order and option order are shuffled at the start of every attempt. The randomization means every attempt is a fresh exam.
What is the pass mark?
The pass mark is 14 of 20 correct answers, or 70 percent. The threshold reflects a working clinical competence in GLP-1 receptor agonist prescribing, not academic mastery. Candidates who score below 14 of 20 receive the full answer key with evidence-cited explanations for every question they were presented and can retake the exam with a freshly randomized question set as many times as needed.
Can I retake the exam?
Yes. There is no limit on retakes. Each attempt draws a fresh random set of 20 questions from the 127-question bank with shuffled option order, so no two attempts are identical. The intent is education first and assessment second. The exam is built as a learning instrument: the full evidence-cited explanation appears on the results screen for every question, whether you answered it correctly or not.
Is this a recognized medical certification?
This is an open physician education initiative published by DermaVue Clinics and authored by Dr. Rejeesh M. Menon, MD. It is not a recognized medical license, specialty board certification, government accredited credential, or CME credit. The certificate reflects completion of a structured self-assessed knowledge evaluation on GLP-1 receptor agonist therapy. It is suitable for personal learning portfolios and for demonstrating engagement with the field, but it does not replace formal medical licensing or board certification.
How are the questions generated?
The 127-question bank was developed by Dr. Rejeesh M. Menon, MD (Internal Medicine, faculty at Washington State University, Medical Director DermaVue Clinics), drawing on primary literature including the ACCORD, DiRECT, ReTUNE, EMPA-REG OUTCOME, DAPA-HF, EMPEROR-Reduced, STEP, SURMOUNT, SUSTAIN, SELECT, FLOW, LEADER, and Counterpoint trial publications, Roy Taylor Twin Cycle hypothesis papers, Daniel Drucker Cell Metabolism reviews, Jens Holst Physiological Reviews papers, ADA Standards of Care 2024, KDIGO Diabetes in CKD 2022, ASA 2023 perioperative guidance, ICMR-INDIAB-17, the Misra consensus 2009, and ICMR PCOS Task Force 2023. Every question carries a peer-reviewed citation.
What topics are covered?
The bank covers seven domains. The paradigm shift in metabolic medicine (ACCORD, Twin Cycle, Counterpoint, DiRECT, ReTUNE, Yajnik thin-fat phenotype, Indian BMI thresholds). SGLT2 inhibitors as proof that glucose is not the disease (EMPA-REG, DAPA-HF, EMPEROR-Reduced). GLP-1 mechanism of action (four pillars, glucose-dependent insulinotropy, POMC and AgRP arcuate signaling, vagal afferents and gastric emptying, mesolimbic reward and food noise, dual GIP/GLP-1 tirzepatide, SELECT, FLOW). Pharmacokinetics and drug design (half-lives, Aib at position 2, C18 fatty acid albumin binding, semaglutide and tirzepatide titration, Rybelsus SNAC absorption, missed dose protocols, Indian generic market after the March 2026 patent expiry). Side effects and safety (nausea via area postrema, MTC and MEN-2, pancreatitis red flag, lean mass loss, gallstones, pregnancy washout, perioperative hold, AKI, hypoglycemia with insulin or sulfonylurea). Special populations (adolescents, type 1 diabetes, CKD, hepatic impairment, PCOS, post-bariatric). History and evolution (Habener 1980s proglucagon work, Gila monster exendin-4, Saxenda 2014).
Do I get a certificate?
Yes. Candidates who score 14 of 20 or higher (70 percent or above) receive a PDF certificate of completion, downloadable from the results screen. The certificate is generated client side using jsPDF, formatted on A4 in horizontal orientation with a gold accent border, and is signed by Dr. Rejeesh M. Menon MD (Internal Medicine, faculty Washington State University, Medical Director DermaVue Clinics) and Dr. Sarath Chandran MD DVL (Managing Director, DermaVue Clinics) with their handwritten signatures embedded. Each certificate carries a unique identifier in the format SH-CERT-XXXXXX for record keeping.