Acquisitions

What are your existing or future plans for business development? Are you anticipating inorganic growth? Do you understand your responsibilities when you acquire another medical device company or you purchase a medical device to round out your product portfolio?

Do you realize that when you make such an acquisition you and your organization inherit any and/all regulatory, quality compliance and liability issues associated with the organization and/or product?

Have you ever had to do a complete product re-design, initiate an extensive product recall, or settle a large claim as a result of an acquisition?

Don’t be unprepared and don’t get caught out in the cold!

Let RQS help you with detailed due diligence of all regulatory and quality compliance issues that will affect your company as a result of an acquisition.

RQS will review all labeling, branding, submissions, registrations, design documentation, product history, quality management system, recalls, and adverse events and make you aware of any and all known and potential issues which you should factor into your decision process.

RQS can also assist or develop an integration and/or transfer plan so that the organization and/or product can be properly integrated into your organization or another site depending on where you want to manufacture and distribute the product.

RQS will help you update any and all associated registrations, filings with regulatory agencies so the integration process is seamless to your organization.

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