Buy Psychedelics: Psilocybin, DMT, LSD, MDMA and Ketamine

Buy Microdosing MDMA Online. The MDMA belongs to the Multidisciplinary Association for Psychedelic Studies (aka MAPS), a nonprofit research organization that does exactly what it sounds like: studies the potential medical benefits of psychedelic drugs. MAPS has investigate LSD, ayahuasca, and ibogaine, too, but the MDMA is specifically used in its ongoing trials of psychedelic-assisted, post-traumatic stress disorder psychotherapy.

Unfortunately, MAPS can’t do much with this stash of Molly. In order for MAPS to move into phase three of its therapy trials in 2017, the Food and Drug Administration requires it to use MDMA that is certified under Good Manufacturing Practices (GMP), which this original batch is not. That means it has to source a brand new kilo of pure MDMA.

Getting your hands on illicit drugs illegally is easy—as simple as firing off a text. But legally acquiring a massive quantity of certified GMP, 99 percent pure, high yield MDMA? That requires a long journey through a labyrinth of regulation, oversight, and bureaucracy.

It all starts with asking the government if you can please buy some psychedelics.

Step One: Getting Permission

“It’s important to remember that they’re not illicit drugs when they’re used in research,” said Dr. John Halpern, a Harvard psychiatrist who has study the effects of peyote and LSD. He note that the difference between a Schedule I drug (like LSD) and a Schedule II drug (like OxyContin) is simply that the latter has been identify for a specific medical purpose. “Otherwise there’s no difference. They’re both equally dangerous,” he said.

But that small difference means research on Schedule I drugs requires a few extra hoops that research on other drugs don’t. The first step is to pen a protocol for a study: a plan for how the researchers intend to conduct their investigation. This protocol is judged by an institutional review board, an independent group that reviews any clinical trials involving humans. If a study involves a Schedule I drug, once the board approves the protocol as ethical, the researchers have to apply for an investigational new drug (IND) number from the FDA.

PURITY;