PremKumar Medical innovations, USA
PremKumar Medical innovations, USA
Engineering and Back-office support services for Medical Device companies
PremKumar, Founder & CEO
We enable medical device companies, clinician innovators, product development engineers focus on innovation by providing Engineering and technical support services that
1) Save you Money - 40%-60% reduction in salary costs
2) Functional teams on ground in US
3) Scalability
4) Meet tight timelines - work can be done 24hrs
5) Excellent communication in English
6) Short-term deployment
7) No long term or "lock-in" contracts
8) Reduce or eliminate the impact of attrition on your company
Contact us today for a free evaluation and no obligation quote for your project.
Referral Reward Program (RRP) - I will be happy to share generous and "forever" commissions on any sales that result from your referrals and customer acquisition efforts.
Engineering services - Both on-site and offshore services available
FDA Remediation services
Medical device manufacturers receive observations (Form 483) and / or warning letters on completion of USFDA Audit. The document outlines any violations of Good Manufacturing Practices (GMP’s) such as the facility, equipment, processes, controls, products, employee practices or records.
Companies require substantial number of unplanned resources, budgets & at the worst are declined an opportunity to sell, shutting down facilities and even prosecution of responsible individuals until the observations are cleared. Companies may also undertake product remediation to resolve issues that they are aware of in their product design and development process.
We assist medical device companies to resolve these observations with efficiency and accuracy. Our experienced and specialized service providers in collaboration with the customer utilize an extensive & comprehensive methodology to complete the remediation project. Our Onshore-Offshore Model with strong project management ensure deliveries with faster timelines, flexible resources and in cost-effective manner.
Process Validation services - Both on-site and offshore services
USFDA approvals for Medical devices
Outcome-Based Delivery Model to provide complete solution from developing engineering documentation to receiving USFDA Approvals & establishment registrations thereafter. Our teams from USA & India collaborate to develop a Cost-Effective Model to complete USFDA Approvals for customers in USA, Europe and Asia.
Complaint handling for post-market activities
Assist companies to develop the mechanism of post-market activities. IZiel assist the companies to document the complaints handling process, help you to understand the objectives of compliant handling within the context of overall Quality System and Corrective and Preventive Action (CAPA) subsystem.
Adopt & implement these steps to help you with compliant handling –
Establishing Complaint Handling System as per legal requirements of ISO 13485, MDR and US regulation for medical devices (CFR 820)
Implementation and support to customer for a particular period
Investigation Training
Root Cause finding and decision making for corrective and preventive action (CAPA)
Developing process for customer feedback and incorporating changes for product improvement.
Establish Complaints Handling System –
Develop procedures for receiving, reviewing, and evaluating complaints by incorporating a formally designated department that ensures:
Process complaints in a uniform and timely manner
Documentation of oral complaints upon receipt
Initial Review and Evaluation –
Guidance to determine whether an investigation is necessary through reviews and evaluation of complaints.
If no investigation is needed, then help to document:
Investigation of Failures –
Guidance & Training to assist companies to conduct thorough review, evaluation and investigation of alleged complaints involving possible failure of a device or labelling/packaging to meet any of its specifications.
Assist with CAPA, as no investigation is required for recurring similar complaints.
Medical Device Reporting –
Evaluation to determine if failure investigation and/or a medical device report (MDR) is required
Help you maintain data in a separate portion of the complaint files or be otherwise clearly identified.
Assist in keeping additional records of investigation in view of:
Records –
Help you maintain records of investigations in consideration to below details, which is a must while complaint handling:
IZiel work with medical device companies to effectively manage Complaints Handling, thereby, help you provide better, safer, more effective & quality product.
Healthcare BPO
Organizations are constantly seeking innovative solutions to enhance efficiency, reduce costs, and improve patient care. One strategy that has gained significant traction is Healthcare Business Process Outsourcing (BPO). This strategic partnership with third-party service providers offers a myriad of benefits, revolutionizing the way healthcare operations are managed. .
Linking US & Asia / ME medical device Businesses, Markets & Talent
Head Quarters: Philadelphia, USA
Asia Office : Chennai, India
Phone : 208-8616488 , WhatsApp : +12088616488
Email: medical@Prem4Biz.com
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