An ISO 9001:2008

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An autonomous research support company, Veeprho Laboratories Private Limited specializes in isolation and purification of impurity by preparative HPLC as well as the custom synthesis of complex molecules. Our client base is spread across the world, most of them being major pharmaceutical companies to whom we supply impurity standards with certification and characterization data. Our main aim is to provide organic synthesis services that are world class and at the same time provide value for money too.
Medicinal Chemistry Services at Veeprho Laboratories :
We offer a variety of services to support pharmaceutical industries to help identify and optimise pre-clinical candidates in the area of small molecules drug discovery. Our senior team members have years of experience in preclinical drug discovery in pharma industry. We are specialised in medicinal chemistry services, custom synthesis and providing innovative building blocks for pharmaceutical industry.

Our services include:
1. Synthesis of focussed libraries
2. Synthesis of Organic Scaffolds
3. Synthesis of NCEs
4. Custom chemical synthesis
5. Synthetic organic chemistry of all major chemotypes
6. Scale up to support in vivo efficacy and toxicity studies
7. Analytical method development
8. Commitment to achieve our customer’s goals

To meet our customer requirements and expectations, our teams provide tailor made research activities. Our discovery support service includes providing medicinal chemistry via FTE. Protecting the IP and respecting the confidentiality of our customers are top priorities at VEEPRHO. Our commitment is to deliver the unsurpassed quality of service and products at competitive prices.

Our expertise offers a unique combination of capabilities in provide complete solution to Pharmaceuticals industry for Impurity standards, Metabolites, Intermediates and APIs.

We provide services to Pharmaceuticals industry having domestic & international clients. Our highly motivated professional team of scientists carry out various syntheses of Impurities/ Metabolites, Intermediates and APIs with quality.

VEEPRHO provides core expertise in Chemistry to their valuable clients and their project demand. We rely on team of our expert scientist to unravel even the most challenging synthetic troubles.

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Client Testimonials
"While dealing with VEEPRHO LABS, I have found Venkat to be very well informed in his areas of specialization and is able to efficiently lead teams that develop for impurity isolation and impurity synthesis. His approach to every situation is systematic and scientific.

His excellent knowledge, dynamic leadership quality and vast experience make him an asset of his organization. I wish him all the success in his professional and personal goals."

-- Dr Sanjay Sonawane, Ex Sr Director-Analytical, SAI LIFE SCIENCES, Pune, Maharashtra, India.
"When we come in contact with VEEPRHO LABS, I found Venkat is instrumental in development and technology transfer of cost effective synthetic schemes of Impurity and impurity isolation.

His time management and project management skills are apt for any organization and he comfortably keeps those deadline without much hiccups. His people management skills are also appreciable. I wish him success for his future."

-- Dr Prabhakar Lahare, Ex Vice President–Analytical R&D, Alembic Research Center, Baroda, Gujarat, India.
Managing Director & CEO

Venkat Shinde

Venkat Shinde is a post graduate in Organic Chemistry. Prior to founding VEEPRHO, he worked as a Sr. Analytical Scientist in Wockhardt Research Center and Glenmark Research Center, Mumbai. He also worked for Nicholas Piramal Research Center, Cadila and Amneal Pharmaceuticals as A-R&D Head.

Venkat has over 18 years of experience in the Pharmaceutical Industry. He has worked in various Pharmaceutical companies, thus having knowledge of US and European regulatory agencies as well as about filing ANDA and DMF, Lab compliances, analytical equipment, formulation process, equipment and other utility equipment. He is also an expert in Research, Manufacturing and Marketing of Pharmaceuticals dosage forms, API, Intermediates and current pharmaceuticals business.

Bupropion | Hydrochlorothiazide | Timolol | Haloperidol | Piroxicam | Ganciclovir | Budesonide | Everolimus | Fulvestrant
Latest News
05 July 2017 : We are glad to announce that we have recently manufactured Piroxicam Impurities like Piroxicam EP Impurity A / 2- Aminopyridine, Piroxicam Impurity B / Piroxicam Desmethyl (CAS No. 65897-46-3), Piroxicam Impurity C / Piroxicam Despyridyl (CAS No. 24683-25-8), Piroxicam Impurity D (CAS No. 6639-62-9), Piroxicam Impurity E (CAS No. 24683-20-3), Piroxicam Impurity F (CAS No. 76508-37-7), Piroxicam Impurity G (CAS No. 35511-14-9), Piroxicam Impurity H (CAS No. 24683-21-4), Piroxicam Impurity I (CAS No. 76508-35-5), Piroxicam Impurity J (CAS No. 35511-15-0), Piroxicam Impurity K / Meloxicam EP Impurity A / Meloxicam Related Compound A (CAS No. 24683-26-9), Piroxicam Impurity L / Meloxicam EP Impurity F / Meloxicam Related Compound C (CAS No. 118854-48-1) etc. It is ready with data. It is confirmed with RT, RRT and RF.
05 July 2017 : We would like to inform you that Veeprho Laboratories is a qualified vendor for certified impurity reference standards. We have recently manufactured Timolol impurities like Timolol Impurity A / Timolol Related Compound A (CAS No. 26839-76-9), Timolol Impurity B / Timolol Related Compound B (CAS No. 59697-06-2), Timolol Impurity C (CAS No. 1391068-18-0), Timolol Impurity D / Timolol Related Compound D (CAS No. 30165-97-0), Timolol Impurity E / Timolol Related Compound E (CAS No. 1026075-53-5), Timolol Impurity F / Timolol Related Compound F (CAS No. 30165-96-9), Timolol Impurity G (CAS No. 75202-36-7), Timolol Impurity H, Timolol Impurity I, Timolol Impurity J etc. It is acceptable to all regulatory agencies in the world like US-FDA, MHRA, MCC, WHO, Brazil and Japan.
05 July 2017 : We are glad to announce that we have recently manufactured Haloperidol impurities like Haloperidol EP Impurity A / Dechloro Haloperidol (CAS No. 3109-12-4), Haloperidol EP Impurity B (CAS No. 1391052-53-1), Haloperidol EP Impurity C, Haloperidol EP Impurity D / Haloperidol Related Compound A (CAS No. 67987-08-0), Haloperidol EP Impurity E, Haloperidol EP Impurity F, 4-(4-Chlorophenyl)- 1,2,3,6 tetrahydropyridine HCl (CAS No. 30005-58-4), Haloperidol-N-oxide (CAS No. 148406-51-3), 4-Fluorobenzoic acid (CAS No. 456-22-4), 4-chloro-1-(4- fluorophenyl)butan-1-one (CAS No. 3874-54-2). We are manufacturer and supplier of Haloperidol Impurities with characterization data along with Certificate of Analysis (COA).