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Pharma Turnkey Project Consultancy



Unicorn Consultants specializing in Pharmaceuticals offers turnkey consultancy services for projects as per WHO, GMP, USFDA, MHRA, TGA and GMP norms and requirements. Our commitment to excellence is evident by the ISO 9001:2000 certification and our expertise is acknowledged by several high profile projects successfully completed in India and abroad.

UCS is one of the leading pharmaceuticals project management consultancy firms providing turnkey solutions for pharmaceutical, biotechnology, health, food, education and hospitality industries.

We offer professional services to clients’ specific requirements and take pride in providing current top quality STATE OF THE ART ENGINEERING CONSULTANCIES.

We are proud to state that the Facilities we have successfully commissioned, in India and Abroad, have complied with the demanding standards and requirements of International companies like conforming to cGMP requirements and US FDA & UK MCA guidelines.


One Stop Solution provider

We undertake comprehensive management of all project activities, right from conception through completion of construction and commissioning, validation, technology transfer, including Continuous Monitoring, thereafter to achieve the projected savings in time and money to add value to our services for the benefit of our clients.We also assist in the up gradation of plants in accordance with the latest industry standards.

Timely Schedule

With the help of specialist consultants for different sections, we are able to achieve the project deadline in less than half time than the competitor hence .TIME SAVING.


With the help of world class principles, we achieve good quality of machines with a double check FAT facility. (First FAT by UCS second by Client) so DOUBLE QUALITY ASSURANCE.

Value Addition

We not only work for our clients but all our endeavour is to create maximum value for our clients, minimise cost and time and deliver projects which exceeds clients expectations.

We Provide not only projects, but can also guide clients for what products to be produced, based on market study

End to End Solutions

We Provide not only projects, but can also guide clients for what products to be produced, based on market study

Flexible for any kind of customisation

Pre Audit:

Unicorn Pharma Consultant assists clients to prepare for an imminent regulatory inspection by carrying out one or more mock regulatory audits in advance of the real thing.

Our consultants will visit the your facility and carry out an inspection in the style of the relevant regulatory body (FDA, MHRA, EMA, Saudi FDA, GCC etc.) after which we provide:

  1. An in-depth, impartial and professional assessment of their current state of compliance.
  2. A detailed, prioritized action plan for the rectification of areas of non-compliance and vulnerability.
  3. Staff coaching in the sorts of questions which are likely to be asked during the inspection and how best to answer them.
  4. Sound, practical support and advice in the run-up to the real inspection.

A few reasons to partner with us

Why Choose US

Starting a project from green field stage to the commissioning level (Turnkey Project) or upgradation of existing facility as per US FDA, UK MHRA, TGA, WHO GMP, ISO 9000 etc., at DCPL you get all services under one roof.

  1. Commitment to Our Clients
    We endeavor to deliver on our commitments to our clients, focusing on transparency, results and high standards. DCPL provides tailor-made solutions to meet clients, business and project goals. We aim to build long-term relationships with our clients that are founded on trust.
  2. Commitment to Quality & Delivery
    We are committed to quality work and on time delivery through the development and implementation of our Quality Management System. UCSPL aims to deliver the highest level of professional excellence.
  3. Experience in Industry
    With over more than 15 projects in India and overseas in the last few years, UCSPL covers a wide variety of pharmaceutical & biotech industries and engineering services.
  4. Commitment to Economic & Sustainable Design
    We at UCSPL emphasize on economical designs with high production & energy efficiency. We believe in sustainable solutions that impart minimal environmental impact.

Salient Features

  1. Experienced, Professional, Focused practical and easy to work with.
  2. We specialize in preparing and handling regulatory submissions for FDA and GCC.
  3. For mock Audit as per MHRA, SFDA and GCC.
  4. Reach out to Global Market.
  5. To have timely and faster dossier preparations and submissions.
  6. For one stop requirements for all your regulatory needs.
  7. Offer concept to commissioning (turnkey projects) of pharmaceutical and CRO facilities.


Delhi Office:
  • 107, RG Square,I.P Ext.Patparganj,
  • New Delhi -110092,India

Noida Office:
  • 740,Tower-B, Plot No. A-40,Sector - 62,
  • Noida 201301 (UP), India

Japan Office:
  • 1-5-9-503, SAILOR KOMATSUGAWA,