Staff Augmentation
Optimize your workforce without long-term commitments
Staff Augmentation
Optimize your workforce without long-term commitments
Collaborating with you to understand your specific staffing needs
G&L specializes in augmenting our clients’ regulatory capabilities through customized contingent staffing solutions. We provide the right technical expertise, in the right location, at the right time.
As regulatory experts across the entire product lifecycle, we support early development, filing strategy, pre- and post-approval CMC, MAA/NDA submissions, publishing, post-approval Lifecycle Management (LCM), and global projects.
Whether you need specific technical skills, temporary workload support, or a comprehensive project team, we are here to discuss your needs and provide tailored solutions.
Benefits include:
- Workload management: We help manage transient peaks in workload, ensuring your operations run smoothly during high-demand periods.
- Project execution: Our teams seamlessly execute project-specific tasks alongside your routine operations, ensuring continuity and efficiency.
- Resource optimization: By refocusing internal resources on revenue-generating activities or core business functions, we help you optimize your workforce.
- Flexible resourcing: Our solutions adapt to evolving business needs, addressing both short- and long-term absences with ease.
- Access to expertise: Gain access to our specialized technical knowledge and global talent pools - our resource is your resource.
- Robust governance: We ensure robust management and governance of external resources, maintaining high standards of compliance and performance.
Thought Leadership
Maximizing efficiency in pharmaceutical regulatory affairs with staff augmentation
Paul Kuiken, Vice President of Advisory Practice at G&L, discusses the case for staff augmentation.
