Services

Scientific

Scientific and technical consulting across nonclinical development, CMC, bioanalytics, and due diligence.

Scientific Consulting Services

Viltis aims to support life sciences companies in the critical areas of research, development, quality assurance, and regulatory compliance. Whether you're developing pharmaceuticals, medical devices, or biologics, our team of experts brings specialized knowledge and hands-on experience to guide your projects from concept to market. We ensure that your products meet the highest scientific and regulatory standards, helping you navigate complex challenges and achieve your innovation goals.

Our pharmaceutical R&D consulting services help you innovate and bring new products to market. We support your scientific teams in developing effective and safe pharmaceutical products.

Our expert team will help you in

: Leading research efforts to develop new pharmaceutical products.

: Crafting and testing formulations to optimize drug delivery systems.

: Conducting chemical analyses to ensure the quality and efficacy of pharmaceutical compounds.

Quality Control Scientist

Implementing rigorous testing procedures to ensure products meet industry standards.

: Monitoring product stability to ensure efficacy over time.

: Conducting microbiological testing to safeguard product safety.

Clinical Research Scientist

Designing and overseeing clinical trials to ensure they are scientifically sound and compliant.

: Applying statistical methods to analyze clinical trial data and support decision-making.

: Studying drug absorption, distribution, metabolism, and excretion to inform dosage and efficacy.

Our scientific consulting services in medical device R&D ensure that your innovations are developed and tested for optimal performance and safety.

Our expert team will help you in

Leading the development and testing of cutting-edge medical devices.

Innovating new materials for use in medical devices, ensuring safety and efficacy.

Biocompatibility Specialist

Ensuring materials and devices are safe for use in humans by verifying biocompatibility.

: Testing devices to ensure they meet stringent quality standards.

Validation Scientist

Validating manufacturing processes and equipment to ensure consistency and reliability.

: Conducting microbiological tests to prevent contamination in medical devices.

: Preparing and submitting regulatory documents to obtain necessary approvals.

: Overseeing clinical trials specific to medical devices, ensuring they meet regulatory standards.

Developing biological products requires specialized expertise. Our consulting services help your R&D teams optimize biologics production processes.

Our expert team will help you in

: Developing and refining processes for the production of biological products.

Conducting cutting-edge research on biological molecules and their interactions.

: Maintaining and optimizing cell cultures essential for biologics production.

: Implementing comprehensive testing protocols to ensure biologics meet quality standards.

Monitoring biological products to ensure they remain stable and effective over time.

: Testing for microbial contamination to guarantee the safety of biological products.

: Managing clinical trials specific to biologics, ensuring they are conducted according to regulatory requirements.

: Analyzing complex data from biologics clinical trials to draw meaningful conclusions.

: Monitoring the safety of biologic products throughout clinical use.

At Viltis, we offer comprehensive pharmacovigilance services to ensure drug safety across all phases of development and post-market monitoring. Our team of

works to detect, assess, and prevent adverse drug reactions, ensuring regulatory compliance and patient safety.

Our pharmacovigilance services include

: Identifying potential safety issues early.

: Developing strategies to minimize potential risks.

: Monitoring and documenting side effects for regulatory bodies.

: Analyzing clinical and post-market data to ensure drug safety.

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How can we help?

Tell us about your program needs and timeline. Our team will respond promptly.

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