Bulk Manufacturing &
Custom Synthesis (BMCS)

We have taken up the challenge to manufacture reagents and powders in bulk scale to meet the critical requirements of several industries that we serve. SRL currently offers more than 2500 PRODUCTS and supports its customers in all phases of the drug manufacturing process, from research, quality control and commercial production, through to providing service in concrete safety and regulatory issues.

We are pleased to investigate and provide a quote for your requirements for any quantity; from milligrams to tons. For Custom Synthesis a realistic minimum order volume depends on many factors, but in principal SRL can help you start with small quantities for laboratory testing, scale up for development, and finally go on to economical continuous manufacturing on the ton scale.

Confidentiality

This is the first step in the BMCS Business, where we value all communications we have with you and make sure that there is clear, transparent & ethical practice of 100% confidentiality with the information you will share with SRL. Irrespective of whether we have a formal secrecy agreement in place with you, SRL will handle your enquiry and other information with the utmost confidentiality. Should you wish to have a formal agreement put in place before disclosing any details, we will be pleased to arrange this.

Customer's Synthetic Route

We examine your requirements based on your own disclosed technical information. If we feel that additional chemistry or analytical testing is required we will discuss this with you and allow for any extra work in the quotation.

SRL In-house Synthetic Route

Where you have no synthetic information about the product required, SRL will use its skills to explore options. Having carefully reviewed these, we will then provide a quotation based on our in-house expertise.

Manufacturing Capability

SRL‘s Bulk Manufacturing and Custom Synthesis (BMCS) business has broadened its production at our Taloja MIDC site to include existing and new bulk fine chemicals which are being manufactured at commercial scales. Production of the raw materials have been on since 2011 at this site and complements the existing offering of highly regulated active and non-active pharmaceutical ingredients manufactured here.

Customer's Synthetic Route

Most of the products manufactured at the Taloja MIDC bulk plant facility meet and exceed IP, BP, USP & Ph. Eur regulation; follow Current Good Manufacturing Practices (cGMPs) for biopharmaceutical production; and comply with International Consortium for Innovation and Quality in Pharmaceutical Development.

Target Audience

We can provide raw materials for various type of Industries some are mentioned below

  • Hormones
  • Beverages
  • Biocides, Insecticides & Crop Sciences
  • Bio-Fermentation (Upstream & Downstream)
  • Biosimilars
  • Blood Plasma
  • Confectionary and Foods
  • Consumer Durables
  • Cosmetics
  • Dairy
  • Diagnostic Kits
  • Electronics
  • Engineering
  • Fast Moving Consumer Goods (FMCG)
  • Formulations (New & Generic)
  • Excipients & Intermediates (Organic & Inorganic)
  • Active Pharmaceutical Ingredients (API) (Human & Veterinary)
  • Vaccines (Human & Veterinary)
  • Neutraceuticals
  • Peptides
  • Injectables
  • Heavy Machinery
  • Antibodies
  • Personal Care Products
  • Protein Purification
  • Specialty Chemicals
  • Home Care & Sanitation
  • Automobile & Aeronautics

POST SALES SUPPORT

SRL not only provides the raw materials through its BMCS program, but we also cater to the strict documentation requirements which our customers ask. Since the last decade, India has become a hub for the regulated as well as the non-regulated pharmaceutical markets, and to serve them we offer complete VQ documents with all the technical, commercial and ethical information that we can provide.

BMCS WORKING

1.

Customer sends new inquiry to SRL

3.

Finalizing the production Process/Synthetic Route

5.

Sampling, Audit & Final Product Approval

7.

Product Dispatch with COA & Documents

2.

Confidentiality Agreement

4.

Submission of Quotation with Terms

6.

Manufacturing and VQ Documentation

8.

After-sales Support if/when required