Callisto Regulatory Consulting provides complete services to the pharmaceutical industry including regulatory and licence applications, pharmacovigilance, manufacturing and API site audits. It also provides assistance with product development and technical transfer projects.
Jo Bunyan has more than 25 years’ experience in the industry. A strong business development professional, she specialises in pharmaceutical regulatory affairs, regulatory submissions, pharmacovigilance and GMP.
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“Annual Renewal Date” means the date 12 months after a Member has signed up to Premium Membership of E2E. “Member” means the contracting party for whom Work is performed by E2E.
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46. In relation to the provision of the Services, it may be necessary or desirable to instruct other professional advisers. You shall be responsible for the appointment of such other professional advisers and for their fees and expenses. Where other professional advisers are appointed E2E will place reliance on their opinion and we will refer to their opinion and our reliance upon it in any Deliverables as appropriate.
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E2E T&C July 2022
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