 PRODUCT REGISTRATION Our consultants can help you to create new product concepts that fill gaps in your portfolio, address product life cycle management, or explore new emerging technologies that impact on your sector and the competitiveness of your products. Increasingly in medtech this requires an understanding of a broad range of technologies which is often beyond the scope of our clients' internal expertise. We can broaden this scope to give reassurance that the 'bigger picture' is being considered. |
 REIMBURSEMENT Strategic planning to obtain the highest reimbursement for your medical device product is crucial for the sales of your medical products. Our expert consultants are experienced with maximizing the reimbursement potential of medical device products. Acquiring a profitable reimbursement price requires not only expertise and familiarity with each market's official reimbursement procedures, but also aggressively reacting to market changes and understanding the government's healthcare goals to justify the pricing for your product accordingly. |
 QUALITY COMPLIANCE Quality systems for medical devices must be performing at the highest standards to eliminate product imperfections and malfunctioning. Many countries today require quality management systems and needs to register, and market your products which are extremely intricate and complex. Life Science is a leader in assisting medical businesses with Asia Quality Control(QC), Quality Assurance(QA), and Quality Management Systems (QMS) that enable them to successfully source, manufacture, and register their products in the market. |
 CLINICAL TRIALS An understanding of the regulatory requirements, having experienced on the ground local team, providing contract research organization services and experience in dealing with each local regulatory authority is essential in administering a smooth, successful clinical trial in the market. Life Science can act as your contract research organization service. |
 QUALITY SYSTEMS DESIGN, IMPLEMENTATION AND AUDITING Our medical device experts have front line experience in terms of managing quality in medtech companies and have helped many clients with ensuring compliance through system design, implementation and auditing. |
 SOURCING AND AUDITING SUPPLIERS Insuring a robust and responsive supply chain is essential to running a successful manufacturing operation. Finding suppliers that meet the required criteria and can add sustainable value requires careful diligence. Our medical device consultants have a deep knowledge of the industry supply chains and can support you in finding and vetting candidates. |
PRODUCT REGISTRATION Our consultants can help you to create new product concepts that fill gaps in your portfolio, address product life cycle management, or explore new emerging technologies that impact on your sector and the competitiveness of your products. Increasingly in medtech this requires an understanding of a broad range of technologies which is often beyond the scope of our clients' internal expertise. We can broaden this scope to give reassurance that the 'bigger picture' is being considered. |
REIMBURSEMENT Strategic planning to obtain the highest reimbursement for your medical device product is crucial for the sales of your medical products. Our expert consultants are experienced with maximizing the reimbursement potential of medical device products. Acquiring a profitable reimbursement price requires not only expertise and familiarity with each market's official reimbursement procedures, but also aggressively reacting to market changes and understanding the government's healthcare goals to justify the pricing for your product accordingly.
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QUALITY COMPLIANCE Quality systems for medical devices must be performing at the highest standards to eliminate product imperfections and malfunctioning. Many countries today require quality management systems and needs to register, and market your products which are extremely intricate and complex. Life Science is a leader in assisting medical businesses with Asia Quality Control(QC), Quality Assurance(QA), and Quality Management Systems (QMS) that enable them to successfully source, manufacture, and register their products in the market. |
CLINICAL TRIALS An understanding of the regulatory requirements, having experienced on the ground local team, providing contract research organization services and experience in dealing with each local regulatory authority is essential in administering a smooth, successful clinical trial in the market. Life Science can act as your contract research organization service. |
QUALITY SYSTEMS DESIGN, IMPLEMENTATION AND AUDITING Our medical device experts have front line experience in terms of managing quality in medtech companies and have helped many clients with ensuring compliance through system design, implementation and auditing. |
SOURCING AND AUDITING SUPPLIERS Insuring a robust and responsive supply chain is essential to running a successful manufacturing operation. Finding suppliers that meet the required criteria and can add sustainable value requires careful diligence. Our medical device consultants have a deep knowledge of the industry supply chains and can support you in finding and vetting candidates. |
 LifeScience is a leader in providing healthcare business development service to the healthcare industry in Asia. We have extensive expertise in helping medical device, pharmaceutical, biotechnology and cosmetic companies achieve compliance with global regulations. |
ㅁ Link | ㅁ Contact Info LifeScience Inc. 15 Hubble, Irvine, CA 92618 info@lfscinc.com |
 LifeScience is a leader in providing healthcare business development service to the healthcare industry in Asia. We have extensive expertise in helping medical device, pharmaceutical, biotechnology and cosmetic companies achieve compliance with global regulations. |
