INDiGO is the fastest and most efficient platform to bring a program from candidate selection through IND and beyond.
Once your clinical candidate is selected, this fully-integrated clinical-enabling package provides inter-disciplinary coordination of all aspects of drug development, conducted and managed by a dedicated Evotec team, and usually at a single Evotec site.
Key features:
- Accelerating your drug discovery and research programs through interdisciplinary integration and expert coordination of all activities “under one roof”
- Industry-leading timelines, taking your program from the selection of an optimal clinical candidate to regulatory submission typically in less than 52 weeks
- Expert management by experienced, dedicated project managers and drug development professionals
- Seamless knowledge transfer across disciplines, maximizing the quality and efficiency of the overall development package
- Custom-designed, flexible development plans that allow for real-time adjustments and adaptability to unforeseeable scientific outcomes
- Excellence in project governance, performance review and issue escalation management
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Tags:
Fact Sheets,
Formulation & CMC,
ADME/DMPK,
IND Enabling Studies/Preclinical Development,
Toxicology & Safety
Download this fact sheet to learn more about formulating your way to successful toxicology studies including:
- Early formulation
- Material science - solid development
- DMPK
- In vitro, in vivo, and in silico models
LEARN MORE
Tags:
Fact Sheets,
Formulation & CMC,
Toxicology & Safety
E.SOLVE is Evotec's solution to accelerate your journey to the clinic supporting your formulation strategy as early as possible from discovery to market approval.
Download this fact sheet to learn more about how E.SOLVE's full range of approaches improve solubilization and bioavailability to ensure that your API can progress through the drug discovery development pipeline faster.
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Tags:
IND Enabling,
Fact Sheets,
Formulation & CMC,
Toxicology & Safety
Learn more about inhalation drug development at Evotec including:
- Integrated and stand-alone development plans tailored to your project
- Formulation development of dry powders and liquids designed to meet a quality target product profile (QTPP) with consideration of final commercial process
- Inhaled analytics, API, material science, cGMP maufacturing and quality assurance processes
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Tags:
Respiratory,
Fact Sheets,
Formulation & CMC
Learn more about biomanufacturing at Just-Evotec Biologics by downloading this presentation first presented at IFPAC in March 2021.
In this presentation, we touch on:
- Historic manufacturing practices
- Macro trends impacting affordability
- Speed and flexible capacity solutions
- New plan design principles
Tags:
Presentations,
Formulation & CMC,
Biologics
