Development of PV Agreements and Safety Data Exchange Agreements

Clear and well-structured agreements are essential for effective pharmacovigilance (PV) collaboration. At MedWatch Consulting, we specialize in drafting, reviewing, and maintaining Pharmacovigilance Agreements (PVAs) and Safety Data Exchange Agreements (SDEAs) that meet global regulatory requirements and protect your organization’s interests.

We ensure that each agreement clearly defines roles, responsibilities, timelines, and data exchange processes between partners, enabling smooth communication and regulatory compliance. Our team has extensive experience supporting licensing deals, co-development projects, distributor partnerships, and global collaborations where PVAs and SDEAs are a cornerstone.

With our guidance, you can establish agreements that provide both compliance and transparency, ensuring that safety information is shared reliably and that patient protection remains the top priority.

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PV support with licensing in/out of products

PV support with licensing in/out of products

We provide PV support for licensing deals, ensuring clear safety agreements and full compliance.

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Acquisition of products or companies

Acquisition of products or companies

We support PV due diligence and integration during product and company acquisitions.

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Co-development agreements

Co-development agreements

We help define PV responsibilities and agreements in co-development partnerships.

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Distributors, agents, and commercial partners in new markets

Distributors, agents, and commercial partners in new markets

We align distributors and partners in new markets with global PV compliance standards.

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Mergers and joint ventures

Mergers and joint ventures

We support PV integration and compliance during mergers and joint ventures.

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KPI development and monitoring

KPI development and monitoring

We design and track KPIs that measure compliance, quality, and efficiency in PV systems.

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