Veol Labs An ISO-13485-2003-company
World Class Medical Device Development Service
Assured Global Quality at low cost
   
   
 
 
 
     
  Services  
    Concept Generation  
     
     
     
   
 
  Product Development  
 
 
We are an ISO 13485: 2003 and ISO 9001:2000 certified organization. Our product development process follows US FDA QSR guidelines of design control. Each of the products being developed passes review stages or "gates" where they are checked for appropriate functioning, completeness and complementation between product processes.
Some of the activities involved in this stage are :
Define & Measure
Analyze
Design
Verify
Validate
Transfer
Each team is adequately staffed and supervised by highly experienced NPD managers. Top management and client are regularly briefed on the progress of their project and feedback sought.
Click here to know more about our
 
 
 
  Pilot Manufacturing  
 
 
Products entering design verification & validation phase needs to have all look, feel, performance characteristics of the final product or should essentially be made with intention of commercial launch.
However, there may be some design or process changes post the verification and validation tests and we understand that pilot manufacturing should be frugal on resources. Our short-run processes and team of vendor partners developed over time passes these criteria very well.
With the skills of our engineers, world class manufacturing facilities and experience, we can make small quantities of products as per your requirement.
Our facilities include :
Semi automatic as well as high pressure Injection Molding.
Extrusion of various polymers such as PA, PU, PP, PC and PE
Clean Room Assembly and Manufacturing.
Packaging and sealing in pouches and trays
Regular processes like milling, grinding, heat-treating, welding and many more.
Electronic Device Assembly.
Eto and access to gamma sterilization facility.
Silicon Molding.
Machining and Fabrication of materials like :
 
Steel (SS 316, SS 304, SS 316 LVM)
MP 35 M
Nanoflex
Nickel-Cobalt
HMWPE / HDPE
Nitinol
Products thus manufactured are highly consistent in their features and performance.
 
 
 
........................................
  NEWS
..............................................
  Veol Labs launches a brand new series of White Papers related to Medical Device Industry, first of which covers the R&D challenges that can be overcome by US Companies by partnering with Indian companies.

Keep watching this space for the next White paper on IP Laws from Indian perspective.
..............................................
  Alliance with ConnIMed Concepts Inc for sales and marketing of product development services in North America
..............................................
  Veol Labs launches Air Embolism Protector, patented and cost effective, for avoiding air embolism.
     
Copyright © 2007. Veol Labs. All rights reserved.
Us Office - Kevin Norris, Email : knorris@connimed.com India, Registered Office - Mangesh Patankar, Email : mp@veollabs.com