Praveen G. Email & Phone Number

Hyderabad, IN

India

Hyderabad, Telangana, India

• Handling of biologics and lyophilization of biologic molecules. Establish stability trends for biologics. Authoring technical protocols, reports, memos, and related regulatory documents to support project goals and.
• Contributing to formulation development and technology transfer to contract research/ manufacturing organizations.
• Knowledge sharing activities to support clinical dosing for Phase 2/3 studies.
• Planning and executing stability studies for… Show more
• Planning and executing stability studies for biologic and nonbiologic programs and summarizing the conclusions in team meetings.
• Deeply understanding the stability data and predicting the shelf of drug products using Minitab® statistical software.

Hyderabad, Telangana, India

• Planning and execution of all activities related to the development and manufacturing of small molecule formulations in support of Nektar pre-clinical and clinical programs by applying DOE principles as applicable.
• Ensure optimal formulation, manufacturing principles, theories, and techniques for product development to deliver phase-appropriate formulations and to support non-GLP and GLP pre-clinical and clinical studies.
• Led and participated in development and… Show more
• Led and participated in development and stability assessment activities, developing IR tablets and lyophilized or liquid formulations for pre-clinical and phase 1 clinical study.
• Developing liquid and solid dosage forms for phase 2/3 clinical studies.
• Participating and representing the team at the group, department, and inter-departmental meetings. Sharing knowledge and expertise of formulation development at cross-functional team meetings.

Hyderabad, Telangana, India

• Ensuring appropriate procedures and standards are followed for the development, manufacture, and stability studies of clinical formulations for Phase I and Phase II trials.
• Designing and executing experiments (pre-formulation, excipient compatibility, development and
• Optimization of formulation, stability studies, and presenting results) in project review meetings.
• Responsible for the preparation of protocols and reports.
• Handling of potent, oncology, and narcotic NCE… Show more
• Handling of potent, oncology, and narcotic NCE molecules. Handling various excipient, moisture sensitive, and hygroscopic NCE molecules and diverse drug product forms. Show less

Hyderabad Area, India

• I developed preclinical formulation to support pharmacokinetic, pharmacodynamic, and toxicology studies. I took care of solubility and bioavailability enhancement of NCE’s having poor solubility properties and.
• Developing preclinical formulation to support pharmocokinetic, pharmacodynamic, and toxicology studies.
• Preclinical formulations and vehicle selection or exclusion for in house and client projects.
• Biopharmaceutical characterization of new chemical entities, etc..
• Plan and execute preformulation studies for drug substances including but not limited to solubility studies, stability studies.
• Be familiar with early phase drug development and have a working knowledge of preclinical candidate characterization to support the drug development program.

M.Pharmacy, Pharmaceutics

B. Pharmacy

D. Pharmacy