Achour law firm provides legal advice to companies and institutions developing medical devices to ensure that clients are well placed to manage the challenges they face to capitalise on opportunities.
To commercialize innovative products, medical devices developers must address issues such as regulatory clearance or approval, patents, financing, manufacturing, and distribution in an increasingly complex global market.
We help clients mitigate risks and pursue opportunities through timely, effective counsel on matters relating to the entire medical-device life cycle. From inception and approval to debut and product maturity, you will benefit from guidance that reflects your business strategies and legal needs.
Our advice in medical devices covers intellectual property, both contentious and non-contentious, mergers and acquisitions, commercial transactions (including licensing and collaborations), capital markets and finance and regulatory matters.
We are positioned to serve developers; manufacturers; researchers; investors; and trade associations. We also work also in the areas of regulatory compliance; health coverage, reimbursement, and pricing; fraud and abuse prevention; legislation and policy; intellectual property; financing; product liability; litigation and investigations; licensing and technology transfer; international trade; and pharmaceuticals and biotechnology.
The firm handles also medical devices disputes. We represent manufacturers of all sizes in contentious proceedings before the courts and regulatory authorities.
We have knowledge to handle litigation and regulatory cases and defend medical devices manufacturers.
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