Pharmaceutical Impurity Supplier
Call Us : +420 774 443 294
Write to us on the following email id to get specific quote venkat@veeprhopharma.com

  • Certified Impurity Reference Standard Manufacturer and Supplier
  • Impurity Standards Supplier
  • Impurity Standards Supplier
  • Impurity Standards Supplier
  • Impurity Standards Manufacturer
  • Impurity Standards
Welcome to Veeprho Pharmaceutical s.r.o Czech Republic, EU
For Impurity Reference standards, VEEPRHO has been recognized throughout Europe, USA and Asia as manufacturer and supplier of certified Impurity Reference standards. VEEPRHO is a high quality manufacturer and distributor of certified Pharmaceutical Impurity Reference Standards. Our facilities in India are GMP and ISO 9001: 2008 certified, All Manufacturing facilities are there in India at Pune and ensuring you precision and reproducibility in results whenever you use products or services produced by VEEPRHO Standards.
Veeprho Pharmaceutical s.r.o is Authorised Distributor of Veeprho Laboratories Private Limited, India.

To meet our customer requirements and expectations, our teams provide tailor made research activities in India. 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 services and products at competitive prices.
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Veeprho Pharmaceuticals s.r.o
Veeprho Pharmaceuticals s.r.o can offer with expert technical support, RRT, RF and other Characterization data 1H NMR, MASS, IR, TGA and HPLC. We have sales offices across the world India, EU and US offering over 5000 Impurity Reference Standards for you to choose from.

The VEEPRHO branded Pharmaceuticals impurity standards specification generally include Chromatographic purity, Water content/volatile matter by TGA and structure confirmation by NMR and IR. Impurity Reference Standards are highly-characterized, physical samples used in testing by pharmaceutical company ensures the identity, strength, quality and purity of medicines. VEEPRHO’s Reference Standard collection consists of more than 5000 impurities and 25-30 new impurity standards are added per month.
About Us
VEEPRHO is an independent research support company specializing isolation and purification of Impurity by preparative HPLC and the custom synthesis of complex molecule. We supply Certified impurity standards with Characterization data, worldwide to client base that includes major pharmaceuticals industry. Our expertise offers a unique combination of capabilities in provide complete solution to Pharmaceuticals industry for Impurity Reference Standards and Metabolites.

We provide services to Pharmaceuticals industry clients. Our highly motivated professional team of scientists carries out various synthesis of Impurities / Metabolites with quality.
Our Team In India
Post doctorate and Post graduate in organic Chemistry are working with us has over 25 years of experience in the Pharmaceutical Industry. They worked in various Pharmaceutical companies, having knowledge of US and European regulatory agencies in filing ANDA and DMF, Impurity isolation, synthesis of impurity, Lab compliances, analytical equipment.


New impurities added in the month of February
Formoterol Impurities : Formoterol Fumarate EP Impurity A
Furosemide Impurities : Furosemide EP Impurity A and Furosemide Impurity B
Leflunomide Impurities : Leflunomide EP Impurity D / Leflunomide BP Impurity D and Leflunomide Metabolite Ethyl Analog
Sulfamethoxazole Impurities : Sulfamethoxazole EP Impurity C and Sulfamethoxazole EP Impurity E
Bupropion | Hydrochlorothiazide | Fulvestrant | Trazodone | Pioglitazone | Ranolazine | Lamotrigine | Budesonide | Carvedilol | Ondansetron | Cinacalcet | Venlafaxine | Darifenacin | Quetiapine | Lidocaine | Aceclofenac | Paracetamol | Metoprolol | Olanzapine | Diphenhydramine | Rufinamide | Propafenone