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Bioavailability/Bioequivalence studies
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Bioequivalance
Bioequivalence

Bioavailability/Bioequivalence

 
Veeda has completed over 700 studies including over 400 bio-studies for major pharmaceutical companies worldwide. We have been audited by several of the world’s leading regulator bodies including 4 times by the USFDA. Over 155 of our complete studies have been for USFDA submission with over 45 of them having FDA ANDA approvals!

Veeda was awarded the 2009 Frost and Sullivan's "Indian Clinical Research Organization of the Year", the 2007 Frost and Sullivan's "Partner of Choice" for phase 1 studies and is the trusted CRO partner to 10 of the world’s top 15 Global Pharmaceutical Companies. Veeda understands Bioavailability/Bioequivalence and has the type of expertise you need in a CRO partner to assure you study is done right!

Veeda has a strong SOP driven culture and ensures compliance with all statutory and mandatory requirements. We provide our clients a dedicated Project Management team to serve as a single, knowledgeable point of contact and a dedicated US Business Development team that is involved and able to assist in all aspects of your studies.
 
Clinical Facilities:
  • 116-beds in 4 temperature controlled clinical investigation areas
  • 12 monitored beds plus two specialist units with 2 beds and 1 bed for intensive monitoring
  • 6 intensively monitored beds at Nadiad, a Clinical Pharmacology Unit dedicated to studies in Renal Impaired Patients and Urology Studies
  • 2 well-equipped, controlled-access, on-site pharmacies
  • In-house catering allowing the Unit to provide for specific dietary requirements
  • MAC 5000 ECG machines, GE wall-mounted monitors
  • Capability to store ECG data in FDA format via a GE MUSE system
  • Infusion pumps & Syringe pumps to carry out Glucose-clamp studies (euglycaemic and hyperglycaemic clamping).
  • GE bicycle ergometer (eBike) to carryout modified stress test.
  • Temperature and humidity controlled archive facilities both on and off site
Veeda’s clinical unit is supported by an in-house laboratory which offers bioanalytical services and operates to the highest regulatory standards. The laboratory is also available to provide stand alone service for clinical work conducted at other sites. Click here for more information on our laboratory services.
Laboratory Facilities:
  • 13 LC/MS/MS with high-throughput HPLC and UPLC
  • Watson LIMS and Tomtec Quadra 96
  • Experienced in handling more than 250 molecules
  • Strong Method Library with over 195 methods
 
 
Bioequivalance
Bioequivalance
 
 
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Ver. 1.70 (Last Updated - 13 Jan 2010)