Frequently Asked Questions
Q. What services does your company offer?
- ABC Cambridge provides a range of consultancy services in the biomedical field, including but not limited to in vitro research, regulatory affairs, in vivo and clinical trial management, quality assurance, and scientific advisory services and consultancy. We also offer contract research services tailored to meet the specific needs of our clients.
Q. How experienced is your team?
- Our team consists of highly experienced professionals with diverse backgrounds in biomedical research, clinical development, regulatory affairs, and other relevant fields. Our experts have extensive experience working with pharmaceutical companies, biotech firms, academic institutions, and regulatory agencies.
Q. Can you assist with regulatory submissions?
- Yes, we have significant expertise in regulatory affairs and can assist with various regulatory submissions, including Investigational New Drug (IND) applications, Clinical Trial Applications (CTA), New Drug Applications (NDA), and Marketing Authorisation Applications (MAA), among others.
Q. Do you provide support for clinical trials?
- Absolutely. We offer comprehensive support for all phases of clinical trials, from study design and protocol development to site selection, patient recruitment, monitoring, and data management. Our goal is to help our clients navigate the complex regulatory landscape and conduct successful clinical trials.
Q. How do you ensure data quality and compliance?
- We have robust quality assurance processes in place to ensure that all aspects of our work meet the highest standards of quality and compliance. Our team adheres to relevant regulations, guidelines, and best practices throughout the project lifecycle to safeguard data integrity and regulatory compliance.
Q. Can you help with scientific writing and publication?
- Yes, we offer scientific writing services to help our clients prepare various documents, including clinical study reports, regulatory submissions, manuscripts, and scientific presentations. Our team includes skilled medical writers with a strong scientific background and expertise in writing for peer-reviewed journals.
Q. What types of clients do you typically work with?
- We work with a diverse range of clients, including pharmaceutical companies, biotech start-ups, medical device manufacturers, academic researchers, and government agencies. Our services are tailored to meet the unique needs of each client, regardless of size or industry focus.
Q. How do you handle confidential information and intellectual property?
- We take confidentiality and intellectual property protection very seriously. We have strict policies and procedures in place to safeguard confidential information and ensure that our clients' intellectual property rights are protected. Our team members are bound by confidentiality agreements and adhere to ethical standards in all interactions.
Q. What geographical regions do you operate in?
- While our headquarters are located in Cambridge, United Kingdom, we provide consultancy and contract research services to clients worldwide. We have experience working across different geographical regions and are familiar with the regulatory requirements and cultural nuances of various countries in Europe, North America, Asia and the Middle East.
Q. How can we get started with your services?
- Getting started with ABC Cambridge is easy. Simply contact us for a free consultation to discuss your specific needs and requirements, and we'll work with you to develop a customised solution tailored to your project goals and timelines.