Life Sciences
We understand Life Sciences much better than others – Our Expertise comes from Experience.
The Life Sciences practice at United Techno is one of the fastest growing industry
verticals in the company. Our Consultants and SME’s have more than 10 years of average
hands on experience in pharmaceutical, biotech and life sciences industry. Our expertise
comes from experiences in multiple domains of the domain which includes US FDA Regulatory
Compliance, Process Validation, Quality Assurance, Quality Audits, Risk Mitigation,
Consent Decree remediation, Computer System Validation and CAPA management.
High quality software delivery capability coupled with our domain expertise helps
clients, larger and medium size, to design and maintain optimized business solutions
which are incompliant to the government regulations. We can help customers to rationalize
costs, enhance operational efficiencies, and improve business agility across all
life sciences business processes.
United Techno has substantial experience in supporting global supply chain processes
in life sciences domain implementing ERP applications like SAP, JDE, MES, CAPA,
Trackwise, LIMS, Filenet, Datacap, ELN and controlled records management solutions
through Documentum and in a validated environment.
Reduce Compliance Cost
United Techno’s highly controlled and well qualified “Offshore Pharma Validation”
process has helped clients control excess validation costs and reduce healthcare
cost. Our Expertise in the cGMP practices and regulatory domain along with IT skills
has helped to make “offshore validation” a reality model in the age of Outsourcing.
We have proven expertise in running validation and compliance projects for fortune
100 companies Biotech and Pharmaceutical companies in North America and Europe.
Industry Expertise
Our pool of life sciences experts helps streamline customer operations end-to-end,
boosting business returns, improving outcomes and applying appropriate compliance
and regulatory controls.
We serve
- Pharma & Biotech industries
- Medical Devices
- Manufacturing & Supply Chain
- Regulatory Compliance