Decentralization of drug clinical trial institutions

1. You asked the right person. Actually, they are all good. In the early stage, the salary of CDC may be higher and the welfare is better. The newly graated freshmen from provincial CDC in the East will make no less than 100000 yuan a year. This kind of unit's employment index is strictly controlled. It doesn't matter how ordinary people can get in. In recent years, the development momentum of drug clinical trials is very hot. In the initial stage, the work in hospital institutions may not be as much as that given by pharmaceutical companies and CDC. But you think, after working in the hospital drug research base for several years, you have so much information in your hand. Based on your experience and information, when you go to a big pharmaceutical factory, your income is not comparable to that of ordinary workers.

2. As for the risk, I would like to explain here that we are doing phase 1 clinical trials, most of the projects are generic drugs,
blood test of phase I clinical trials
to give the simplest example, Harbin No.6 pharmaceutical factory is making money selling erythromycin, and Baiyunshan Pharmaceutical also wants to sell erythromycin, so it has done this thing, but new drugs must go through the process of marketing, Therefore, the instry of pharmacists was born

the so-called phase 1 clinical trial is not symptomatic. It mainly compares the absorption and metabolism of marketed drugs and generic drugs. The dosage is generally very small, which is smaller than the dosage you usually take for fever, cold, headache and diarrhea. Generally, there are only one or two tablets in a cycle, and then blood samples are taken for test
if you ask me if there will be any toxic side effects or risks, I will tell you that all Western medicines have toxic side effects. To talk about the toxic side effects is to play a hooligan. If you drink too much water, you will be poisoned
when you say risk, there is no risk in what you do. From workers to drivers, risks in daily life are everywhere. I can only say that this thing is far less terrible than you think. Hospitals, pharmaceutical companies and medical staff have already reced the risk to the minimum
I've seen a lot of people talk about the Japanese poisoning a lot of people by doing experiments with Chinese people. I can't help laughing. What's the age when the rule of law society, pharmaceutical companies, hospitals and medical staff are not responsible for accidents every day? Legal projects, regular hospitals
, if you are short of money, you will come. It is not a long-term livelihood, but it can solve the urgent need.

3. What does PD mean in drug clinical trials<

PD refers to pharmacodynamics
i.e. pharmacokinetics of drug effect.

PK refers to pharmacokinetics
i.e. pharmacokinetics.
PD refers to pharmacodynamics
i.e. pharmacokinetics of drug effect.

PD refers to pharmacodynamics
i.e. pharmacokinetics of drug effect.
PK refers to pharmacokinetics
i.e. pharmacokinetics of drug effect PK refers to pharmacokinetics, i.e. pharmacokinetics.
refers to the relationship between drug concentration and time

4.

flying speed cro answers for you:

there must be harm. It's the third part of poison

absolute safety can not be guaranteed, but the premise of clinical trials of new drugs is to ensure that the drugs have passed the safety study, but also does not rule out the occurrence of clinical adverse reactions not written in the instructions

It is necessary to sign an agreement, and the interests of both parties will be clearly marked on it. The clinical purpose is to prove that in a certain number of cases, the applicable symptoms in the instruction manual are completely correct

If you give more or less subsidies, it depends on what drugs you are testing. It's unreasonable to give 20000 yuan for cold medicine and 20000 yuan for cancer targeted medicine

as mentioned above, we can't guarantee 100% safety, and the probability of insecurity is very low. I've been CRC for three years, but I haven't seen any problems. Personality guarantee

there are so many questions to answer for the time being. You can continue to ask

5. It is true that drug clinical trial is a scientific research to evaluate the efficacy and safety of a certain drug or treatment scheme, and its purpose is to find better drugs and treatment schemes. Participants can have free access to research drug treatment, especially for cancer patients, which means new treatment hope.

6. You have asked too many questions. I suggest you go to some well-known pharmaceutical forums, such as pharmaceutical intelligence forum, to find some information or ask questions

7. In the process of drug clinical trial, it involves the links of sample collection, transportation, analysis, data processing, etc. any link involving foreign affairs has been approved by the human genetics office, such as the sponsor, cro company, SMO company, cold chain transportation company, sample testing company, data management and statistics company, etc, Any company entrusted by the sponsor with foreign background has applied to the human genetics office