Research and Development of drugs through preclinical testing

GXP Quality Systems facilitates advanced and innovative discoveries of drugs. After thorough research and development of the drug preclinical research is initiated. The expert team of GXPQS Biotech Preclinical Research Texas put all their efforts, learning, experience, and hard work with dedication. Preclinical Research is a long term process. Research may go for 12 to 14 years. The actual development of drugs starts with preclinical Research itself. All safety measures and concerns are determined efficiently and effectively.

How do GXP experts work in Preclinical Research Phase?

Determining the discovery of module or compound, the pre-clinical testing phase takes place that includes the following phase’s i.e.

1. Technique and Quantity of making drug:

The perfect and advanced technique is determined to know about the absorption, toxicity, and excretion intake of drugs in the human body. The quantity rate is also decided in this phase, how much quantity to be of the drug should be released in the market.

2. Dosage Intake:

The percentage of dosage is tested to know the accurate amount of drug intake in the human body.

3. Side Effects:

Testing on animals and humans (if required) goes side by to know if there are any side effects regarding the intake of double dosage and many more concerns that can give side effects to the human body. Al side effects are identified.

4. Risk Analysis:

Risk Analysis takes place to know if some unusual activity occurs how much risk should be there. What risk will be there if a drug is consumed by a patient who is already on another medication or treatment? All risk factors are analyzed before launching the product publicly.

5. Regulations and Approvals:

All regulations and legal advisories are followed while going through these phases and approval of higher authorities like the World Health Organization and other authorities are taken into consideration for QA review.

Final Reports, regular submission, and assessment are reviewed by higher health authorities, and then it is approved by them.

6. Launch of the Product:

Last but not the least, going through all these phases finally a medicine/product is launched in the market publically to cure the diseases of human beings.

This process is only possible with highly skilled experts who know, and experience in this field. Our team is one of them, experienced, skillful, and highly efficient towards their work.