Ensure medicines involved in clinical trials meet UK compliance standards with comprehensive investigational drug services that enhance equitable access and participation in research.
Are you confident that your clinical trial's pharmaceutical management meets all UK regulatory requirements and supports equitable patient participation?
Many clinical trials face delays due to inadequate pharmaceutical preparation, inconsistent IMP handling, or insufficient patient education about trial medications.
Regulatory bodies require robust clinical pharmacy systems that not only ensure safety and compliance but also enhance accessibility for diverse patient populations through proper investigational drug services.
Nclusiv offers comprehensive pharmacy assurance and clinical trial pharmacy services to ensure medicines meet UK compliance standards while supporting equitable access and participation in research.
We offer a completely free introductory discussion call to address your individual clinical pharmacy needs.
Clinical trial pharmacy assurance encompasses the comprehensive management of investigational medicinal products (IMPs) throughout the research process.
Our clinical pharmacy services ensure proper handling, storage, dispensing, and monitoring of trial medications while maintaining regulatory compliance and supporting patient safety.
Could inadequate medication blinding or randomisation processes compromise your trial integrity?
Are your study protocols designed with optimal feasibility and regulatory compliance for clinical pharmacy management?
Are your dosage preparation and dispensing procedures meeting the highest standards for investigational drug safety?
How effectively are trial participants understanding their medication requirements through proper clinical pharmacy counselling?
Are you capturing and reporting all adverse events appropriately through robust pharmacovigilance systems?
Could improved clinical trial pharmacy processes enhance patient engagement and trial retention?
How might streamlined investigational drug management reduce overall clinical trial costs and timelines?
Expert Protocol Development Support — We offer specialist design and review of study protocols for clinical pharmacy feasibility and regulatory compliance.
Reliable Medication Blinding and Randomisation — Our robust clinical pharmacy processes maintain the integrity of blinded studies throughout the trial duration.
Accurate IMP Dispensing and Preparation — Precise preparation and dispensing of investigational drugs per study protocols with full documentation.
Enhanced Patient Understanding — Comprehensive patient education and counselling services through expert clinical pharmacy support to improve medication compliance.
Rigorous Pharmacovigilance — Continuous monitoring and reporting of adverse events to ensure patient safety throughout the clinical trial.
Regulatory Compliance Support — Expert guidance on UK pharmaceutical regulations and MHRA requirements for clinical trial medicines.
Secure IMP Handling — Proper storage, handling, and inventory management of investigational products throughout the trial period.
Patient-Centric Clinical Pharmacy Services — Enhanced support systems that improve patient experience and trial accessibility.
Our Pharmacy Assurance Process
1. Protocol review and development — We assess your pharmaceutical requirements and provide expert input on protocol design and feasibility
2. Medication preparation systems — We establish robust blinding, randomisation, and preparation procedures for your investigational products
3. Patient education programme — We develop comprehensive support materials and counselling systems to enhance patient understanding
4. Safety monitoring implementation — We establish pharmacovigilance systems for continuous adverse event monitoring and reporting
5. Compliance verification — We ensure all pharmaceutical management meets UK regulatory standards and requirements
6. Ongoing support delivery — We provide continuous pharmaceutical support throughout your trial duration with real-time inventory management
Download our comprehensive service brochure for detailed information on our methodology, case studies, and pricing:
Our comprehensive pharmaceutical support can be tailored to address different aspects of your trial needs:
Protocol Development Support — Expert design and review of study protocols for clinical pharmacy feasibility and compliance
Medication Blinding and Randomisation — Reliable systems to maintain trial integrity through proper IMP management
Dispensing and Dosage Preparation — Accurate preparation and dispensing of investigational drugs per protocol requirements
Patient Education and Counselling — Comprehensive clinical pharmacy support to improve patient understanding and medication adherence
Pharmacovigilance Services — Continuous monitoring and reporting of adverse events for optimal patient safety
Regulatory Compliance Support — Expert guidance on UK requirements for clinical trial pharmaceutical management
Inventory Management Systems — Real-time tracking and management of investigational product supplies
We believe that excellent clinical pharmacy management enhances both trial integrity and patient experience, making clinical research more accessible and effective for everyone.
Expert Pharmaceutical Management — Our clinical pharmacy specialists bring extensive experience in trial pharmaceutical requirements and UK regulatory compliance.
Comprehensive Regulatory Compliance — We ensure your trial meets all UK standards for pharmaceutical management and safety monitoring.
Secure IMP Handling and Storage — Robust systems for proper handling, storage, and tracking of investigational products throughout your trial.
Customised Clinical Pharmacy Solutions — Our services are tailored to your specific trial requirements, therapeutic area, and patient population needs.
Real-Time Inventory Management — Advanced systems for tracking investigational product supplies and ensuring continuous availability.
Patient-Centric Services — Enhanced support systems that improve patient experience and accessibility throughout the trial.