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Anna Ridderstad Wollberg

Senior projektledare

Tel

+46 10 516 60 61

Email

anna.ridderstad.wollberg@ri.se

Location

Stockholm

Unit

Formulering (101301)

Ask me about

Ask me about

Knowledge base for Swedish vaccine production

RISE has led the assignment Vinnova received from the government (Registration number: N2020 / 03157) with the aim of analyzing how Sweden's innovation and production capacity for vaccines and other biological drugs compares …

Nordic Life Science Days 2022

Nordic Life Science Days is the largest Nordic partnering conference dedicated to the life science industry. Come meet our experts in pharmaceutical development at the event in Malmö 28-29 September.

Future Pharmaceutical Development

Pharmaceuticals are becoming ever more complex in their structures and activities and therefore demand new competencies, new capacities and to some extent new interpretations of regulatory requirement. What are these emerging need…

Support for healthcare during the crisis

Within RISE, there is cutting-edge expertise that can serve as support for healthcare and its suppliers during the current crisis. We can offer support and advice in, among other things, drug production and drug development, medic…

Guide to drug development – from target to patient

The development of a drug is an expensive and resource-intensive process and it is therefore important, from the beginning, to meticulously plan ahead for all necessary steps in the journey towards the new product. A well-structur…

Vaccin and non-cliical safety

RISE can help with the design and execution of the non-clinical safety testing for vaccine from characterisation through formulation and safety studies to the approval by regulatory agencies. Toxicologists and immunologists can pl…

Toxicological tests and safety

We can test and assess the potential toxicities/hazards of emerging drug candidates, industrial chemicals, food additives and medical devices, contributing to safety assessments required for market approvals. We can also support i…

In vitro methods for toxicology

Our wide selection of in vitro models help you confirm and optimise pharmacological effects, to predict and analyse toxic effects and to study ADME properties of drugs in different phases of development. Toxicological assessment o…

Pharmaceutical Development

At RISE we know the entire pharmaceutical development chain, from target to patient. We can help with process development, analysis (GMP/GLP), formulation and production (GMP) of the pharmaceutical product for clinical trials, but…