Years of expertise in fermentation science have led to the development of specialized knowledge, enabling progression in the nutraceutical industry, and exploring sectors beyond traditional pharmaceutical realms while embracing sustainability to uphold a green and healthier future.
Our commitment to high quality is demonstrated through our all-encompassing Contract Manufacturing (CMO) and Contract Development and Manufacturing (CDMO) services, with our state-of-the-art greenfield fermentation facility with 4 x 100 KL capacity.
Read MoreYears of fermentation expertise
CDMO Capacity
Pipeline Products
Countries
R&D Centres
Manufacturing Sites
It is fully equipped and compliant with Good Manufacturing Practices (GMP), designed to facilitate the commercialization, strain improvement, media optimization, process development from upstream to downstream, and scaling of our products.
Our services encompass the scaling of processes from laboratory scale within our R&D facilities to a commercial scale of 100 KL, in addition to aiding in strain development, optimizing downstream efficiency, and
With a mission to create regulatory processes that prioritize compliance for pharmaceutical products, catering to a wide range of global markets. The R&D team consists of highly skilled scientists, including postdoctoral researchers, PhD graduates, and postgraduates. They are committed to developing complex active pharmaceutical ingredients (APIs) by leveraging expertise in biotechnology, analytics, regulatory affairs, and intellectual property.
Read MoreFacilities that are state-of-the-art and certified by the US FDA and EU-GMP (German Bavaria) are equipped to handle all forms of bacteria, yeast, or fungi, producing active ingredients or intermediates while upholding the highest quality standards throughout the production process.
A diverse selection of fermentors, from lab scale to the largest 100KL capacity, provides you with the flexibility to choose the appropriate manufacturing scale for your API development and production at the best cost.
We focus on advanced technologies and research to lead the industry. Our dedication to innovation enables us to provide sophisticated solutions for managing microbial strains and cultures, while effectively controlling various process parameters in your API development and manufacturing.
Understanding the intricate world of pharmaceutical regulations is a key part of what we offer. We deliver extensive regulatory assistance to simplify the product approval process.
We are dedicated to clean, green, and sustainable manufacturing as we construct our cutting-edge greenfield nutraceutical fermentation facility, set to be operational by early 2025.
We utilize a vegan-friendly fermentation method that produces sustainable, high-quality active ingredients for drugs and nutraceuticals. Our advanced equipment operates within a compliant regulatory framework, ensuring safety and efficacy. This scalable process improves the bioavailability of compounds derived from plants and marine sources, paving the way for innovative wellness and therapeutic solutions while minimizing ecological impact.
CORPORATE OFFICE AND UNIT – I
385, Pigdamber,
Rau, Indore,
MP, India 453331
+91-731-6676405 | 6676406
+91-731-4201222
symbiotec@symbiotec.in
UNIT - II
Plot No. 5,6,7 & 8,
Special Economic Zone,
Phase II, Pithampur, Indore,
MP, India 454755
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