Minimalist IAS
2018 GS Paper III

UPSC CSE (Main) 2018 · GS Paper III · Question 15

Why is there so much activity in the field of biotechnology in our country? How has this activity benefitted…

Syllabus line: IT, space, robotics, biotech & IPR — “Awareness in the fields of IT, Space, Computers, robotics, nano-technology, bio-technology and issues relating to intellectual property rights.”

GS Paper III 2018 · Q15

15 marks · 250 words IT, space, robotics, biotech & IPR

Why is there so much activity in the field of biotechnology in our country? How has this activity benefitted the field of biopharma?

Approach · directive: “why / how”

What it asks · Explain why biotechnology has grown so fast in India (skills, policy, demand) and how that has helped biopharma: vaccines, biosimilars and low-cost drugs.

The question has 2 parts — answer each

  1. Why: reasons for the high level of biotechnology activity in India — skills, industry base, demand and policy
  2. How: how this activity has benefited biopharma — vaccines, biosimilars, affordable drugs and exports, with the remaining challenges

Open with · India combines a large scientific workforce, a strong pharma base, big health and farm needs and supportive policy, which has made biotechnology one of its fastest-growing knowledge sectors.

Cover

  • Drivers: a large pool of trained scientists and low-cost research, rich biodiversity, an established generic pharma industry, and big needs in health, food and energy.
  • Policy push: the Department of Biotechnology (1986), the National Biotechnology Development Strategy (2015-20), BIRAC (2012) for start-ups and industry, incubators and biotech parks, and Make in India.
  • Farm and industrial biotech: Bt cotton since 2002, biofertilisers and biopesticides, tissue culture, enzymes and biofuels, though the debate on genetically modified crops continues.
  • Biopharma gains: India is a leading vaccine maker; indigenous vaccines such as Rotavac, affordable insulin, monoclonal antibodies, biosimilars and diagnostics lower prices and support exports.
  • Regulation and IPR: product patents since 2005 pushed firms towards innovation; guidelines on similar biologics (2012, revised 2016) opened the biosimilar route.
  • Challenges: thin early-stage funding, slow approvals, imported inputs and equipment, weak translational research, biosafety and the ethics of clinical trials.

Close with · India's biotech surge rests on skills, policy and demand; sustaining biopharma's gains needs more research funding, faster regulation and strong IPR and biosafety frameworks.

Question: UPSC's CS (Main) 2018, GS Paper III — paper ↗. Approach: Minimalist IAS, checked 30 Sept 2026 (how we verify) — UPSC publishes no model answers. ·

Model answer · 279 words (UPSC limit 250) · Minimalist IAS

India pairs a large scientific workforce and a strong generic-pharma base with big needs in health, food and energy and a supportive policy framework; together these have made biotechnology one of its fastest-growing knowledge sectors.

Why so much activity

  • People and cost: a large pool of trained biologists, chemists and engineers, and research at a fraction of Western cost.
  • Industry base: an established generic pharmaceutical industry with manufacturing scale and regulatory experience, ready to move into biologics.
  • Demand: a large disease burden, the need for affordable vaccines and drugs, food security and biofuels create domestic markets.
  • Policy: the Department of Biotechnology (1986), the National Biotechnology Development Strategy 2015-20, BIRAC (2012) funding start-ups and industry-academia projects, biotech parks and incubators, and Make in India.
  • Resources and farm use: rich biodiversity; Bt cotton since 2002, biofertilisers, biopesticides and tissue culture, though the debate on GM food crops continues.
  • IPR: product patents since 2005 pushed firms from copying towards innovation.

How biopharma has benefited

  • Vaccines: India is a leading vaccine maker for the world; indigenous products such as Rotavac show research-to-market capability.
  • Biosimilars: guidelines on similar biologics (2012, revised 2016) opened a regulated path; Indian firms make affordable insulin and monoclonal antibodies, cutting prices at home and building exports.
  • Diagnostics and enzymes: low-cost diagnostic kits and industrial enzymes widen access and lower healthcare costs.
  • Ecosystem: BIRAC grants and incubators have created a pipeline of biopharma start-ups.

Challenges

  • Thin early-stage funding, slow approvals, dependence on imported inputs and equipment, weak translational research, and biosafety and clinical-trial ethics.

India's biotech surge rests on skills, policy and demand; sustaining biopharma's gains needs more research funding, faster and predictable regulation, and strong IPR and biosafety frameworks.

Written by Minimalist IAS from facts checked at source (how we verify) — a little fuller than exam length, so every part of the question is covered; in the hall, keep the structure and trim the detail. UPSC publishes no model answers: compare your structure and coverage with this, then write your own.

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