Danna Ross
About
Danna Ross is from Fuquay-Varina, North Carolina, United States. Danna works in the following industries: "Pharmaceuticals". Danna is currently Pharmaceutical Development Consultant at Independent Consultant. In Danna's previous role as a Vice President Inhalation Drug Development at Cardinal Health, Danna worked in until Mar 2006. Prior to joining Cardinal Health, Danna was a Senior Technical Manager, US Inhalation Drug Delivery at 3M Pharmaceuticals and held the position of Senior Technical Manager, US Inhalation Drug Delivery. Prior to that, Danna was a US Department Manager, Inhalation Drug Delivery at 3M Pharmaceuticals from May 1999 to Jul 2001. Danna started working as UK Department Manager, Inhalation Drug Delivery, 3M Health Care at 3M Pharmaceuticals in Aug 1999. From Apr 1998 to May 1999, Danna was Technical Manager, Inhalation Drug Delivery at 3M Pharmaceuticals. Prior to that, Danna was a Technical Supervisor, Inhalation Drug Delivery at 3M Pharmaceuticals from Jun 1997 to Apr 1998. Danna started working as Research Specialist, Inhalation Technology at 3M Pharmaceuticals in Nov 1994.
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Danna Ross's current jobs
• Assist respiratory companies with product development to gain regulatory approval. (Data review and recommendation of next steps, project planning, assessment of probability of success and completeness of program.) • Assist in regulatory correspondence and meetings around CMC issues. • Develop proof of concept in vitro programs to evaluate/market devices to potential partners. • Develop program management systems for small companies. • Assist virtual companies with program management/coordination of programs with CROs. • Device assessment • Assist small companies with organization structure, training, GMP requirements to achieve successful product development. • Due diligence of CROs and manufacturing facilities
Danna Ross's past jobs
Operations and strategic responsibility for the inhalation group providing development and analytical services for all inhalation dosage forms (metered dose inhalers, dry powder inhalers, nebulizer solutions, nasal sprays, and novel inhalation delivery systems). Oversight of clinical supply manufacturing for inhalation products including MDIs, DPIs, nasal, and specialty inhalation products.
3M Management Positions April 1998 to November 2002 Responsible for budgeting, resourcing, technical review of global projects, strategic planning for Global Inhalation Drug Delivery, and developing and maintaining appropriate systems to ensure ongoing compliance with GMPs, SOPs, safety, and training. Areas of scientific oversight included technology assessment, NCE and partner feasibility, development, scale-up and support of marketed inhalation products. Operations and strategic responsibility for US Inhalation Drug Delivery Product Development, Analytical Research and Development, and Marketed Product Support.
May 1999 to August 1999; July 2000 to July 2001 Operations and strategic responsibility for US Inhalation Drug Delivery Product Development and Marketed Product Support
Operations and strategic responsibility for UK Inhalation Drug Delivery Product Development (including formulation and devices), Process Development, and Neotechnic Limited Valve Development.
Operations and strategic responsibility for US Inhalation Drug Delivery Product Development; global CMC team leader for HFA aerosol project.
Global CMC team leader for HFA aerosol project; matrix responsibility for 12 workteams with over 80 members including personnel from aerosol R&D, analytical R&D, regulatory, quality assurance, operations, aerosol manufacturing at 2 sites, valve R&D, and valve manufacturing.
Group leader in aerosol systems development; formulation development of HFA aerosols, novel surfactant development, breath-actuated device development; powder preformulation; and aerosol valve development. Global technical team leader for a HFA breath-actuated metered dose inhaler. Team leader for an interdivisional team developing physical and biological models to assess the deposition and fate of aerosolized compounds. Developed and presented Aerosol Technology Conferences for the continuing education of respiratory physicians.
Formulation development of HFA aerosols and dry powder device development; served as technical liaison with partner companies (both US and European based).
PHARMACY EXPERIENCE: Relief Pharmacist; Revco Drug Store January 1986 to January 1988 Pharmacist Manager; Revco Drug Store; Belton, MO August 1980 to December 1985 Staff Pharmacist; Truman Medical Center West; Kansas City, MO October 1979 to August 1980