Research and Development (R&D)
Optimizing Innovation and Compliance
At BioBoston Consulting, our R&D services are uniquely positioned to enable Life Sciences firms to effectively manage through the complex landscape of Product Development while navigating Compliance with Regulatory Standards. Our R&D operation has the skill and expertise to offer Strategic Consulting support for every step in the R&D workflow with an innovative and efficient emphasis.
Why Choose Us for R&D?
Strategic Guidance
We offer professional advice in smoothing the R&D process, right from ideation to product development, ensuring it aligns with Regulatory Requirements and the best practices of the industry.
Compliance Assurance
Our team is knowledgeable in Regulatory Standards; hence, all R&D activities are directed toward and in full Compliance with applicable Regulations to minimize risks and delays.
Innovation Focus
We enforce innovation while maintaining Compliance and enable customers to be abreast of the latest challenges in an ever-changing industry environment.
Proven Results
Our success in R&D projects has built trust with clients across the Life Science Industry.
Our R&D Services Include:
- Ideation and Concept Development
- Feasibility Studies
- Product Development Strategies
- Regulatory Compliance Assessments
- Risk Management Planning
- Innovation Consulting
Ready to Transform Your R&D Process?
Contact us today to learn more about our Research and Development services and how we can help you achieve innovation while assuring regulation.
All Services
- Quality Assurance and Regulatory Compliance
- Investigational New Drug (IND) Application
- Regulatory Strategy & Submissions
- Investigational Device Exemption (IDE) Application
- Vendor Selection & Qualification
- Project & Risk Management
- Technology Transfer
- Quality Management Systems (QMS)
- Gap Assessment and Remediation
- Funding and Investment Strategies
- Research and Development (R&D)
- Biostatistics and Data Analysis
- Lab Operations and Efficiency
- Medical Writing
- CDMO Vendor Selection Qualification & Oversight
- CRO Selection & Qualification
- CTO Selection & Qualification
- Data Integrity and Software Implementation
- Clinical Operations
- Clinical Trial Monitoring
- FDA Inspection Readiness
- Internal and Supplier Audits
- Regulatory CMC Support
- Qualification and Validation
- GxP Training
- Computer System Validation (CSV)
- Strategic Advising
- Process Optimization
- Health Authority Meeting Support
- Recruitment