Innovative Solutions and Trusted Expertise in API Manufacturing

We understand that in the complex world of pharmaceuticals, the journey can be challenging. That’s why our commitment is to make this journey easier for you by providing high-quality APIs.

Welcome to the core of pharmaceutical manufacturing. Here at SCL, we value being your trusted partner as a CDMO/CMO/CRO in the domain of API manufacturing. We understand that in the complex world of pharmaceuticals, the journey can be challenging. That’s why our commitment is to make this journey easier for you by providing high-quality APIs, specialty and performance chemicals, and advanced intermediates. Our product range includes high-potent molecules and niche generics, all backed by high compliance certifications, including CEP, USFDA, Japanese PMDA, etc.

We recognize the criticality that our clients face in ensuring a reliable and time-bound delivery of their pharmaceutical products. Being true partners to our Customer is a key value for SCL and we exercise the best of customer service, flexibility, and deliver solutions that not only meet your immediate needs but also contribute to the long-term success of your organisation.

From raw material procurement, chemical synthesis, isolation and purification, to QC and packaging, we offer unwavering commitment to quality and safety. Our USP is a strong backward integrated product range, which empowers us to manufacture the key raw materials intrinsic to our products, guaranteeing a seamless supply chain, thus assuring unparalleled quality and economic efficiency.

Our commercial APIs are sold across the globe, from Europe and United States to Japan, Korea, Brazil, Turkey Russia & CIS countries, South & Central America, Middle East & Northern Africa regions. At our state-of-the-art Knowledge Centre in Hyderabad, we provide reliable API support, ensuring timely and essential contributions at critical stages of your API product manufacturing and sales. This support ensures that your company can advance confidently through every phase of development and market introduction.

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Our manufacturing facility is KFDA approved, WHO GMP, WCC certified, cGMP certified and ISO 9001:2015 certified. Our R&D facility is capable of developing non-infringing APIs.

Specialized API Production Capabilities at Saurav Chemicals

Accredited by global regulatory bodies such as the US FDA and EU GMP, our facilities uphold the highest standards in API synthesis, safety, and sustainability.
Our Small Volume Facility encompasses a KG Scale & Pilot Facility with equipment ranging from 63 L to 1000 L, specifically tailored for the production of low volume, high-value APIs.
This specialized space adheres to cGMP standards and supports high-potency API (HPAPI) production, ensuring precise and secure manufacturing processes.
Our facility is also utilized for regulatory filings with authorities like USFDA, PMDA, and EDQM, reflecting our commitment to compliance and quality across all operations.

Process

Our process for high-quality best API, Advanced intermediates and Specialty chemicals development include

Chemical Synthesis

Purification and Isolation

Quality Control and Testing

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