Transforming
Healthcare

Pharmaceutical Ingredients

Laurus stands as a global leader in the supply of anti-retroviral APIs and intermediates, playing a pivotal role in increasing access to affordable medicines worldwide. Our advanced yet cost-effective technologies in this crucial segment align with the goal of providing quality pharmaceuticals to patients globally.

In the realm of oncology, Laurus excels, offering an extensive range of APIs with facilities equipped to handle high-potent materials at both developmental and commercial scales. Our commitment extends to expanding our portfolio in diabetes, ophthalmology, and cardio-vascular therapy areas, focusing on making a difference and establishing leadership.

For contract development and manufacturing (CDMO) of APIs and intermediates, we provide globally compliant cGMP facilities coupled with our expertise in chemistry. Recognized as a preferred partner for Contract Research and Manufacturing Services (CRAMS), we attribute our success to stringent quality and Environmental, Health, and Safety (EHS) systems, a broad operability range, robust project management practices, and extensive contract manufacturing experience. With proven capabilities, Laurus delivers end-to-end API solutions to global markets that not only meet but exceed quality, regulatory, intellectual property (IP) requirements, and cost targets.

We offer our globally compliant cGMP facilities, along with our chemistry expertise, to customers for contract development and manufacturing of APIs and intermediates. We are already a preferred CRAMs partner to several customers, owing to our stringent quality and EHS systems, wide operability range (from grams to multi-tonnage scale), robust project management practices, and vast contract manufacturing experience.With proven capabilities, we provide an end-to-end API solutions to global markets that meet and exceed the quality, regulatory and IP requirements as well as cost targets.

Infrastructure

What sets Laurus' manufacturing infrastructure apart is the rigorous standardization of quality and systems across all sites, ensuring a uniform standard for all markets. This uniformity, coupled with equivalent infrastructure across multiple facilities, guarantees seamless business continuity.

Capabilities

Technologies

In alignment with our developmental infrastructure, Laurus' manufacturing facilities are designed to be future-proof, incorporating complementary infrastructure for evolving technologies and platforms.

High-Potent Development

Apart from non-potent compounds, Laurus boasts one of the largest capacities for handling potent, Hi-Potent compounds—those with OEL between 1-10ug/m³ TWA8Hrs.

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Resolution and Separation

While Laurus Labs prioritizes innovative chemistry and intelligent process development to avoid separations at scale, we recognize that regulatory constraints can sometimes hinder rapid process changes.

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Flow Chemistry

In recent years, Laurus Labs has progressively enhanced its capabilities in flow chemistry at scale. This complements continuous-flow chemistry (CFC) processes developed in our R&D facilities for both our portfolio products and client projects.

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Bio-Catalysis

In alignment with emerging trends in pharmaceutical manufacturing, Laurus Labs made early investments in dedicated capacities for handling bio-catalytic processes. Our state-of-the-art infrastructure includes large-volume reactors, some with capacities up to 20KL.

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Hazardous Process Manufacturing

Laurus Labs boasts multiple sites equipped to handle High-Energy & Hazardous Reactions, including processes like Grignard synthesis, metal halides reactions, and high-pressure hydrogenation.

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Particle-Size Alteration

As a fully integrated pharmaceutical manufacturer, Laurus Labs ensures the flexibility to alter particle sizes of drug substances to meet diverse formulation requirements.

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Solutions

At Laurus Labs, we extend our expertise through comprehensive contract and custom manufacturing solutions, allowing client organizations to outsource various stages of the manufacturing process. Our offerings cover the production of proprietary or generic Active Pharmaceutical Ingredients (APIs), intermediates, and, in certain cases, starting materials.

Custom Manufacture Generic APIs

Our approach involves chemical process design, development, optimization, analytical method development and validation, process safety studies, kilo-lab runs, critical process parameter evaluation, technology document preparation, tech transfer to the plant, plant-scale process validation by R&D, filing of Drug Master File (DMF), and ultimately commercial-scale manufacturing and supply.

Custom Manufacture Proprietary APIs, Intermediates

Aligned with the total development approach outlined in the R&D section, our scope encompasses chemical process design, development, optimization, analytical method development and validation, process safety studies, kilo-lab runs, critical process parameter evaluation, technology document preparation, tech transfer to the plant, plant-scale process validation by R&D, regulatory filing (CMC) support for DMF filing by the client, and final commercial-scale manufacturing and supply.

Contract Manufacture Tech-transfer projects APIs, Intermediates, SMs

Handling tech-transfer projects, we take responsibility for all aspects of manufacturing, including sourcing raw materials, adhering to Good Manufacturing Practices (GMP), ensuring product quality, and guaranteeing effective delivery.

Clinical-scale Manufacturing - APIs, Intermediates, Specialty Ingredients, etc.

Whether utilizing a client-provided process or developing a chemical process and analytical development from scratch, Laurus Labs offers a comprehensive solution for clinical drug substance manufacturing, covering toxicological evaluation to Phase-III clinical trials. Our commitment lies in providing tailored solutions for your success

Products

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