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	Licensing and Partnering
	Mammalian Cell Line Development
	Metabolic stability testings
	Metabolite identification/characterisation
	Multi-gene production system
	Operation services for all stages of drug development
	Permeability Screening Using Caco2 Monolayers
	Pharmacodynamic studies
	Pharmacology, Non-clinical Safety, Bio-analysis
	Pharmacovigilance
	Physical properties analysis of pharmaceutical raw materials – APIs and excipients, and drug products, including DSC and LD techniques
	Plasma Stability
	Pre-clinical virus safety testing
	Preparation of Marketing Authorization Application documents (CTD Module 3) for drug products, according to FDA/EMA requirements
	Process Research and Development
	Radiochemical Synthesis
	Rational design and directed evolution of enzymes
	Regulatory: Submission of Clinical Trials for authorization, elaboration of documents for submission to authorities and ethics committees.
	Routine DNA analysis of animal and micro-organisms
	Selection of recombinant antibodies against custom targets from PD libraries

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